Engineering of an antibody for tumor-selective binding of cd47

ABSTRACT

Antibodies are provided which comprise at least one Fab portion that binds CD47 and at least one Fab portion that binds the tumor associated antigen (TAA) CD20; wherein the Fab portion that binds CD47 exhibits low affinity for CD47; and, wherein the Fab portion that binds CD20 exhibits high affinity for CD20; and, wherein the antibody selectively binds CD47 and blocks CD47 interaction with SIRPα in tumor cells while exhibiting no substantial binding to CD47 in normal cells.

FIELD OF THE INVENTION

Provided herein are tumor-selective antibodies, pharmaceutical compositions, and methods of use for the treatment of pathological conditions effected by cells undergoing aberrant proliferation, including hematological oncology conditions, hematological malignancies, lymphoproliferative disorders, B-cell disorders, B-cell malignancies, and B-cell lymphoma.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is entitled to priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 62/830,335, filed Apr. 5, 2019, which is hereby incorporated by reference in its entirety.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. The ASCII copy, created on Mar. 26, 2020, is named 298068-314_Sequence_Listing.txt and is 407 kilobytes in size.

BACKGROUND OF THE INVENTION

Over the past decade, the use of blocking agents against inhibitory immune checkpoints has been one of the most significant advances in anticancer treatment (Sharpe A H. Introduction to checkpoint inhibitors and cancer immunotherapy. Immunol Rev. 2017 March; 276(1):5-8). The exciting results obtained with CTLA-4 and PD-1 blockade led to the evaluation of several innate immune checkpoints that could be targeted in anticancer treatment, in particular pathways regulating macrophage function. Macrophages express SIRPα which interacts with CD47, a ubiquitously expressed protein that mediates a “don't eat me” signal that functions to inhibit phagocytosis. Expression of CD47 confers resistance to phagocytosis of antibody-bound tumor cells by macrophages. In the absence of CD47 binding to SIRPα, antibodies that can bind Fc-receptor on macrophages can enhance phagocytosis of these cells. Cancer cells have evolved to hijack this interaction by upregulating the expression of CD47 on their cell surface, thus counterbalancing pro-phagocytic signals and increasing the chances of evading innate immune surveillance (Matlung H L, Szilagyi K, Barclay N A, van den Berg T K. The CD47-SIRPα signaling axis as an innate immune checkpoint in cancer. Immunol Rev. 2017 March; 276(1):145-164). Therefore, blockade of the CD47-SIRPα interaction represents a promising therapeutic strategy to activate the phagocytic clearance of tumor cells from the body. Several SIRPα-CD47 blocking agents, including humanized and fully human anti-CD47 antibodies, anti-SIRPα antibodies, soluble SIRPα dimers fused to the Fc portion of human IgG, high-affinity monomeric SIRPα devoid of Fc portion, and camelid-derived monomeric fragments of anti-CD47 antibodies (nanobodies), have shown efficacy in vitro and in preclinical studies against various types of human tumors (Veillette A, Chen A., SIRPα-CD47 Immune Checkpoint Blockade in Anticancer Therapy. Trends in Immunology, 2018, 39(3):173-184). Some of the SIRPα-CD47 blocking agents, including CC-90002 (anti-CD47), Forty Seven's anti-CD47 (Hu5F9-G4) and Trillium's SIRPα-fusion Fc have been tested in phase I and phase II clinical trials, respectively (Veillette A, Tang Z. Signaling Regulatory Protein (SIRP)α-CD47 Blockade Joins the Ranks of Immune Checkpoint Inhibition. J Clin Oncol. 2019 Feb. 27:JCO190012). These approaches in the clinic are limited by the need for combination therapy (e.g., rituximab), the tissue sink (i.e., presence of non-tumor cells to which the therapeutic antibody binds, thus decreasing the bioavailability of the antibody for tumor cells) in targeting CD47 with a high-affinity binder, and the observed hematologic toxicity with some of the clinical molecules (anemia, neutropenia, and/or thrombocytopenia). Importantly, while protein therapeutics are indeed explored to treat a number of diseases, biopharmaceutical entities can prompt an immune response involving production of anti-entity antibodies when administered to subjects which result in reduced efficacy and/or toxicity.

SUMMARY OF THE INVENTION

The present invention is directed to an antibody comprising at least one Fab portion that binds CD47 with low affinity and at least one Fab portion that binds CD20 with high affinity; wherein the bispecific antibody selectively binds CD47 in tumor cells and is substantially free of binding to CD47 in normal cells.

Fab portions described herein that bind CD47 with low affinity generally exhibit affinity for CD47 between about 0.1 μM and about 25 μM, for example, when measured as Kd (dissociation constant) by surface plasmon resonance (SPR). Fab portions described herein that bind CD47 with low affinity exhibit affinity for CD47 from about 0.25 μM to about 20 μM. Certain preferred embodiments exhibit affinity for CD47 from about 0.4 μM to about 4.0 μM. Certain embodiments exhibit affinity for CD47 from about 1 μM to about 3.0 μM. In some embodiments, for example, the Fab portion that binds CD47 exhibits an affinity for CD47 that is from about 0.1 μM to about 5.0 μM. In some embodiments, the Fab portion that binds CD47 exhibits an affinity for CD47 that is from about 0.1 μM to about 0.2 μM, 0.3 μM, 0.4 μM, 0.5 μM, 0.6 μM, 0.7 μM, 0.8 μM, 0.9 μM, 1.0 μM, 1.1 μM, 1.2 μM, 1.3 μM, 1.4 μM, 1.5 μM, 1.6 μM, 1.7 μM, 1.8 μM, 1.9 μM, 2.0 μM, 2.1 μM, 2.2 μM, 2.3 μM, 2.4 μM, 2.5 μM, 2.6 μM, 2.7 μM, 2.8 μM, 2.9 μM, 3.0 μM, 3.1 μM, 3.2 μM, 3.3 μM, 3.4 μM, 3.5 μM, 3.6 μM, 3.7 μM, 3.8 μM, 3.9 μM, 4.0 μM, 4.1 μM, 4.2 μM, 4.3 μM, 4.4 μM, 4.5 μM, 4.6 μM, 4.7 μM, 4.8 μM, 4.9 μM or about 5.0 μM.

In some embodiments, the Fab portion that binds CD47 exhibits an affinity for CD47 that is from about 0.2 μM to about 4.0 μM. In further embodiments, the Fab portion that binds CD47 exhibits an affinity for CD47 that is from about 0.5 μM to about 3.5 μM. In further embodiments, the Fab portion that binds CD47 exhibits an affinity for CD47 that is from about 1.0 μM to about 3.0 μM.

The present invention is further directed to an antibody comprising at least one Fab portion that binds CD47 and at least one Fab portion that binds CD20; wherein the Fab portion that binds CD47 exhibits low affinity for CD47; and wherein the Fab portion that binds CD20 exhibits high affinity for CD20; and, wherein the bispecific antibody selectively binds CD47 in tumor cells and is substantially free of binding to CD47 in normal cells; and, wherein the antibody activates antibody-dependent cellular phagocytosis of the tumor cells which express CD20.

The present invention is further directed to an antibody comprising at least one Fab portion that binds CD47 and at least one Fab portion that binds CD20; wherein the Fab portion that binds CD47 exhibits low affinity for CD47; and, wherein the Fab portion that binds CD20 exhibits high affinity for CD20; and, wherein the bispecific antibody selectively binds CD47 in tumor cells and is substantially free of binding to CD47 in normal cells; and, wherein the antibody mediates complement-dependent cytotoxicity (CDC) of the tumor cells which express CD20.

The present invention is further directed to an antibody comprising at least one Fab portion that binds CD47 and at least one Fab portion that binds CD20; wherein the Fab portion that binds CD47 exhibits low affinity for CD47; and, wherein the Fab portion that binds CD20 exhibits high affinity for CD20; and, wherein the bispecific antibody selectively binds CD47 in tumor cells and is substantially free of binding to CD47 in normal cells; and, wherein the antibody mediates antibody-dependent cellular cytotoxicity (ADCC) of the tumor cells which express CD20.

The invention is further directed to monomeric elements of the IgG1 1+1 heterodimers described herein which contain certain light chain (LC) and heavy chain (HC) constant regions that drive the production of the IgG1 1+1 heterodimer format. In one embodiment, an anti-CD47 LC constant region that reduces LC mispairing during production comprises SEQ ID NO:340. In another embodiment, an anti-CD47 HC constant region that ensures heterodimer formation of the Fcs during production comprises SEQ ID NO:342. In another embodiment, an anti-CD20 LC constant region that reduces LC mispairing during production comprises SEQ ID NO:344. In another embodiment, an anti-CD20 HC constant region that ensures heterodimer formation of the Fcs during production comprises SEQ ID NO:346.

The invention is further directed to an antibody wherein the Fab portion that binds CD47 is derived from VL (SEQ ID NO:325) and VH (SEQ ID NO: 326) regions of anti-CD47 species CC-90002 wherein the binding affinity for CD47 is substantially attenuated and the immunogenicity is substantially reduced.

The invention is further directed to a bispecific antibody wherein the anti-CD47 VL is derived from SEQ ID NO: 325 and exhibits 1-7 amino acid substitutions relative to SEQ ID NO:325; and, the anti-CD47 VH is derived from SEQ ID NO: 326 and exhibits 141 amino acid substitutions relative to SEQ ID NO:326 wherein the binding affinity for CD47 is substantially attenuated and the immunogenicity is substantially reduced.

The invention is further directed to a bispecific antibody wherein the anti-CD47 VL is derived from SEQ ID NO: 325 and exhibits 1-7 amino acid substitutions relative to SEQ ID NO:325 wherein at least one (1) amino acid substitution in the anti-CD47 VL (SEQ ID NO: 325) is selected from the group consisting of A10S, M11L, K24R, A51E, N52S, L54F, and 556D; (substitutions in the anti-CD47 VL are numbered relative to the first amino acid of the VL) and, the anti-CD47 VH is derived from SEQ ID NO: 326 and exhibits 1-11 amino acid substitutions relative to SEQ ID NO:326 wherein at least one (1) amino acid substitutions in the anti-CD47 VH (SEQ ID NO: 326) is selected from the group consisting of T14P, Q43K, A44G, E59Y, D66G, M76T, S84R, S88A, M93V, S102E, and T115L (substitutions in the anti-CD47 VH are numbered relative to the first amino acid of the VH).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD47 comprises (i) a light chain variable region (VL) region selected from the group consisting of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:5, SEQ ID NO:7, SEQ ID NO:9, SEQ ID NO:11, SEQ ID NO:13, SEQ ID NO:15, SEQ ID NO:17, SEQ ID NO:19, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:29, SEQ ID NO:31, SEQ ID NO:33, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:53, SEQ ID NO:55, SEQ ID NO:57, SEQ ID NO:59, SEQ ID NO:61, SEQ ID NO:63, SEQ ID NO:65, SEQ ID NO:67, SEQ ID NO:69, SEQ ID NO:71, SEQ ID NO:73, SEQ ID NO:75, SEQ ID NO:77, SEQ ID NO:79, SEQ ID NO:81, SEQ ID NO:83, SEQ ID NO:85, SEQ ID NO:87, SEQ ID NO:89, SEQ ID NO:91, SEQ ID NO:93, SEQ ID NO:95, SEQ ID NO:97, SEQ ID NO:99, SEQ ID NO:101, SEQ ID NO:103, SEQ ID NO:105, SEQ ID NO:107, SEQ ID NO:109, SEQ ID NO:111, SEQ ID NO:113, SEQ ID NO:115, SEQ ID NO:117, SEQ ID NO:119, SEQ ID NO:121, SEQ ID NO:123, SEQ ID NO:125, SEQ ID NO:127, SEQ ID NO:129, SEQ ID NO:131, SEQ ID NO:133, SEQ ID NO:135, SEQ ID NO:137, SEQ ID NO:139, SEQ ID NO:141, SEQ ID NO:143, SEQ ID NO:145, SEQ ID NO:147, SEQ ID NO:149, SEQ ID NO:151, SEQ ID NO:153, SEQ ID NO:155, SEQ ID NO:157, SEQ ID NO:159, SEQ ID NO:161, SEQ ID NO:163, SEQ ID NO:165, SEQ ID NO:167, SEQ ID NO:169, SEQ ID NO:171, SEQ ID NO:173, SEQ ID NO:175, SEQ ID NO:177, SEQ ID NO:179, SEQ ID NO:181, SEQ ID NO:183, SEQ ID NO:185, SEQ ID NO:187, SEQ ID NO:189, SEQ ID NO:191, SEQ ID NO:193, SEQ ID NO:195, SEQ ID NO:197, SEQ ID NO:199, SEQ ID NO:201, SEQ ID NO:203, SEQ ID NO:205, SEQ ID NO:207, SEQ ID NO:209, SEQ ID NO:211, SEQ ID NO:213, SEQ ID NO:215, SEQ ID NO:217, SEQ ID NO:219, SEQ ID NO:221, SEQ ID NO:223, SEQ ID NO:225, SEQ ID NO:227, SEQ ID NO:229, SEQ ID NO:231, SEQ ID NO:233, SEQ ID NO:235, SEQ ID NO:237, SEQ ID NO:239, SEQ ID NO:241, SEQ ID NO:243, SEQ ID NO:245, SEQ ID NO:247, SEQ ID NO:249, SEQ ID NO:251, SEQ ID NO:253, SEQ ID NO:255, SEQ ID NO:257, SEQ ID NO:259, SEQ ID NO:261, SEQ ID NO:263, SEQ ID NO:265, SEQ ID NO:267, SEQ ID NO:269, SEQ ID NO:271, SEQ ID NO:273, SEQ ID NO:275, SEQ ID NO:277, SEQ ID NO:279, SEQ ID NO:281, SEQ ID NO:283, SEQ ID NO:285, SEQ ID NO:287, SEQ ID NO:289, SEQ ID NO:291, SEQ ID NO:293, SEQ ID NO:295, SEQ ID NO:297, SEQ ID NO:299, SEQ ID NO:301, SEQ ID NO:303, SEQ ID NO:305, SEQ ID NO:307, SEQ ID NO:309, SEQ ID NO:311, SEQ ID NO:313, SEQ ID NO:315, SEQ ID NO:317, SEQ ID NO:319, and SEQ ID NO:321; and,

(ii) a heavy chain variable region (VH) region, selected from the group consisting of SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:12, SEQ ID NO:14, SEQ ID NO:16, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32, SEQ ID NO:34, SEQ ID NO:36, SEQ ID NO:38, SEQ ID NO:40, SEQ ID NO:42, SEQ ID NO:44, SEQ ID NO:46, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68, SEQ ID NO:70, SEQ ID NO:72, SEQ ID NO:74, SEQ ID NO:76, SEQ ID NO:78, SEQ ID NO:80, SEQ ID NO:82, SEQ ID NO:84, SEQ ID NO:86, SEQ ID NO:88, SEQ ID NO:90, SEQ ID NO:92, SEQ ID NO:94, SEQ ID NO:96, SEQ ID NO:98, SEQ ID NO:100, SEQ ID NO:102, SEQ ID NO:104, SEQ ID NO:106, SEQ ID NO:108, SEQ ID NO:110, SEQ ID NO:112, SEQ ID NO:114, SEQ ID NO:116, SEQ ID NO:118, SEQ ID NO:120, SEQ ID NO:122, SEQ ID NO:124, SEQ ID NO:126, SEQ ID NO:128, SEQ ID NO:130, SEQ ID NO:132, SEQ ID NO:134, SEQ ID NO:136, SEQ ID NO:138, SEQ ID NO:140, SEQ ID NO:142, SEQ ID NO:144, SEQ ID NO:146, SEQ ID NO:148, SEQ ID NO:150, SEQ ID NO:152, SEQ ID NO:154, SEQ ID NO:156, SEQ ID NO:158, SEQ ID NO:160, SEQ ID NO:162, SEQ ID NO:164, SEQ ID NO:166, SEQ ID NO:168, SEQ ID NO:170, SEQ ID NO:172, SEQ ID NO:174, SEQ ID NO:176, SEQ ID NO:178, SEQ ID NO:180, SEQ ID NO:182, SEQ ID NO:184, SEQ ID NO:186, SEQ ID NO:188, SEQ ID NO:190, SEQ ID NO:192, SEQ ID NO:194, SEQ ID NO:196, SEQ ID NO:198, SEQ ID NO:200, SEQ ID NO:202, SEQ ID NO:204, SEQ ID NO:206, SEQ ID NO:208, SEQ ID NO:210, SEQ ID NO:212, SEQ ID NO:214, SEQ ID NO:216, SEQ ID NO:218, SEQ ID NO:220, SEQ ID NO:222, SEQ ID NO:224, SEQ ID NO:226, SEQ ID NO:228, SEQ ID NO:230, SEQ ID NO:232, SEQ ID NO:234, SEQ ID NO:236, SEQ ID NO:238, SEQ ID NO:240, SEQ ID NO:242, SEQ ID NO:244, SEQ ID NO:246, SEQ ID NO:248, SEQ ID NO:250, SEQ ID NO:252, SEQ ID NO:254, SEQ ID NO:255, SEQ ID NO:258, SEQ ID NO:260, SEQ ID NO:262, SEQ ID NO:264, SEQ ID NO:266, SEQ ID NO:268, SEQ ID NO:270, SEQ ID NO:272, SEQ ID NO:274, SEQ ID NO:276, SEQ ID NO:278, SEQ ID NO:280, SEQ ID NO:282, SEQ ID NO:284, SEQ ID NO:286, SEQ ID NO:288, SEQ ID NO:290, SEQ ID NO:292, SEQ ID NO:294, SEQ ID NO:296, SEQ ID NO:298, SEQ ID NO:300, SEQ ID NO:302, SEQ ID NO:304, SEQ ID NO:306, SEQ ID NO:308, SEQ ID NO:310, SEQ ID NO:312, SEQ ID NO:314, SEQ ID NO:316, SEQ ID NO:318, SEQ ID NO:320, and SEQ ID NO:322.

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD20 comprises anti-CD20 VL CDRs RASSSVSYIH (CDRL1; SEQ ID NO:353), ATSNLAS (CDRL2; SEQ ID NO:354), QQWTSNPPT (CDRL3; SEQ ID NO:355); and, VH CDRs SYNMH (CDRH1; SEQ ID NO:356), AIYPGNGDTSYNQKFKG (CDRH2; SEQ ID NO:357), STYYGGDWYFNV (CDRH3; SEQ ID NO:358).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD20 comprises anti-CD20 LC (SEQ ID NO:331) and anti-CD20 HC (SEQ ID NO:332).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD47 comprises a light chain variable region (VL) region comprising VL CDRs QASQDIHRYLS (CDRL1; SEQ ID NO:359), RESRFVD (CDRL2; SEQ ID NO:360), and LQYDEFPYT (CDRL3; SEQ ID NO:361); and a heavy chain variable region (VH) region comprising VH CDRs DYYLH (CDRH1; SEQ ID NO:362), WIDPDQGDTYYAQKFQG (CDRH2; SEQ ID NO:363), AYGESSYPMDY (CDRH3; SEQ ID NO:364).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD47 comprises a light chain variable region (VL) region comprising a VL CDRs RASQDIHRYLS (CDRL1; SEQ ID NO:365), RESRFVD (CDRL2; SEQ ID NO:366), LQYDEFPYT (CDRL3; SEQ ID NO:367); and a heavy chain variable region (VH) region comprising VH CDRs DYYLH (CDRH1; SEQ ID NO:368), WIDPDQGDTYYAQKFQG (CDRH2; SEQ ID NO:369), AYGESSYPMDY (CDRH3; SEQ ID NO:370).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD47 comprises a light chain variable region (VL) region comprising VL CDRs RASQDIHRYLS (CDRL1; SEQ ID NO:371), RANRLVS (CDRL2; SEQ ID NO:372), LQYDEFPYT (CDRL3; SEQ ID NO:373); and a heavy chain variable region (VH) region comprising VH CDRs DYYLH (CDRH1; SEQ ID NO:374), WIDPDQGDTYYAQKFQG (CDRH2; SEQ ID NO:375), AYGESSYPMDY (CDRH3; SEQ ID NO:376).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD47 comprises VL (SEQ ID NO:317); and VH (SEQ ID NO:318).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD47 comprises VL (SEQ ID NO:319); and VH (SEQ ID NO:320).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD47 comprises VL (SEQ ID NO:321); and VH (SEQ ID NO:322).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD47 comprises LC (SEQ ID NO:333) and HC (SEQ ID NO:334).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD47 comprises LC (SEQ ID NO:335) and HC (SEQ ID NO:336).

The invention is further directed to a bispecific antibody wherein the Fab portion that binds CD47 comprises LC (SEQ ID NO:337) and HC 1367 (SEQ ID NO:338).

In addition, the current invention is directed to a pharmaceutical composition for the control of tumor cells, for administration to a patient in need thereof, comprising a bispecific entity described herein.

In addition, the current invention is directed to a pharmaceutical composition for the treatment of a B-cell disorder or a B-cell malignancy, for administration to a patient in need thereof, comprising a bispecific entity described herein.

The invention is further directed to a method of controlling tumor cells comprising administering an effective amount of a bispecific entity described herein to a patient in need thereof.

Further the invention is directed to a method treatment of a B-cell disorder or a B-cell malignancy comprising administering an effective amount of a bispecific entity described herein to a patient in need thereof.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a schematic illustration of certain attributes of bispecific entities described herein engineered to overcome the challenge of ubiquitous CD47 expression including low affinity binding without avidity to CD47; minimal binding to normal cells, i.e., no tissue sink; high affinity selective avidity binding to CD20 which results in selective binding to tumor cells. TAA: Tumor Associated Antigen

FIG. 2 illustrates an example bispecific entity architecture, protein engineering features, and several biopharmacological attributes.

FIGS. 3A-3C show that example species bispecific entities described herein induce macrophage-mediated phagocytosis of CD20+CD47+ OCI-Ly3 NHL cells. FIGS. 3A-3B are graphs that show the percentage of phagocytic macrophages in view of antibody concentration. FIG. 3C is a table showing KD and EC50 values for bispecific species described herein.

FIGS. 4A-4C show that example bispecific entities, CD47×CD20 IgG1 species, described herein demonstrate CDC function. FIGS. 4A-4B are graphs that show CDC in view of antibody concentration. FIG. 4C is a table showing average EC50 values for TPP-1360, TPP-1362 and rituximab.

FIGS. 5A-5C show that example bispecific entities, CD47×CD20 IgG1 species, described herein demonstrate potent ADCC function in CD20 high NHL cells, i.e., significantly higher than rituximab. FIGS. 5A-5B are graphs that show cytotoxicity in view of antibody concentration. FIG. 5C is a table showing CD20/CD47 Ratio.

FIG. 6 illustrates example architecture of bispecific entities described herein as well as features of certain examples.

FIG. 7 shows an example species bispecific entity described herein, TPP-1360, that substantially shifted the binding signal to B-cells and rather weakly to T cells, monocytes, and NK cells, with minimal or no binding to platelets or red blood cells as compared to binding of TPP-23 (408_437 Fab (VL: SEQ ID NO:899; VH: SEQ ID NO:900) with IgG1), thereby illustrating selective binding to B-cells in human whole blood.

FIG. 8 illustrates an example species bispecific entity described herein, TPP-1360, that is demonstrated to selectively bind CD47⁺/CD20⁺ Raji Cells but not CD47⁺/CD20⁻ human red blood cells (RBCs).

FIG. 9 shows that, in a co-culture of Raji cells and human RBCs, an example species bispecific entity described herein, TPP-1360, displayed dose-dependent binding to CD47⁺/CD20⁺ Raji cells but no binding to human RBCs, even at concentration as high as 1 mg/mL.

FIG. 10 illustrates that TPP-1360, for example, potently and completely blocked recombinant human SIRPα-Fc binding to human CD47 expressed on the surface of CD20⁺/CD47⁺ lymphoma cell line OCI-Ly3.

FIG. 11 illustrates that TPP-1360, for example, potently and completely blocked recombinant human SIRPα-Fc binding to human CD47 expressed on the surface of CD20⁺/CD47⁺ lymphoma cell line Raji.

FIG. 12 illustrates that treatment with TPP-1360, for example, induced macrophage-mediated phagocytosis of the CD20⁺ malignant B cell line, Raji.

FIG. 13 illustrates that treatment with TPP-1360, for example, induced macrophage-mediated phagocytosis of the CD20⁺ malignant B cell line, OCI-Ly3.

FIG. 14 illustrates that treatment with TPP-1360, for example, induced macrophage-mediated phagocytosis of the CD20⁺ malignant B cell line, REC-1.

FIG. 15 illustrates that treatment with TPP-1360, for example, induced macrophage-mediated phagocytosis of the CD20⁺ malignant B cell line, RIVA.

FIG. 16 shows that treatment with TPP-1360, for example, triggered significantly more efficient phagocytosis than rituximab in Raji and OCI-Ly3 cells, likely due to the concomitant blockade of the SIRPα-CD47 interaction and the engagement of activating receptors, such as FcγRs, by TPP-1360.

FIG. 17 shows binding of rituxan and bispecific antibodies such as TPP-1360, for example, to Raji cells (CD20⁺/CD47⁺) as measured by surface plasmon resonance (SPR).

FIG. 18 shows the EpiMatrix antibody immunogenicity scale.

FIG. 19 shows treatment with TPP-1362 and rituxan in a Raji xenograft model.

FIG. 20 shows treatment with TPP-1360 and rituxan in a Raji xenograft model.

FIG. 21 illustrates that TPP-1360 and TPP-1362, for example, potently and completely blocked recombinant human SIRPα binding to human CD47 expressed on the surface of CD20⁺/CD47⁺ lymphoma cell line OCI-Ly3. Rituxan was found to have no effect on SIRPα binding.

DETAILED DESCRIPTION OF THE INVENTION

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of skill in the art to which this invention belongs. All publications and patents referred to herein are incorporated by reference.

As used herein, the articles “a” and “an” may refer to one or to more than one (e.g. to at least one) of the grammatical object of the article.

As used herein, “about” may generally refer to an acceptable degree of error for the quantity measured given the nature or precision of the measurements. Example degrees of error are within 5% of a given value or range of values.

Embodiments described herein as “comprising” one or more features may also be considered as disclosure of the corresponding embodiments “consisting of” and/or “consisting essentially of” such features.

As used herein “low affinity for CD47” refers to an affinity for CD47 that is below about 25 μM, for example from about 0.05 μM to about 25 μM when measured in vitro as Kd by SPR.

As used herein “high affinity for CD20” refers to an affinity for CD20 that is at or above about 0.4 nM, for example, from about 0.4 nM to about 12 nM. In some embodiments, “high affinity for CD20” refers to an affinity for CD20 that is from about 0.4 nM to about 5 nM.

Bispecific entities described herein selectively bind CD47 on tumor cells and are substantially free of binding to CD47 in normal cells. As used herein “substantially free of binding to CD47” generally refers to binding less than 5% of CD47 on (CD20−/CD47+) normal cells. Bispecific entities described herein bind less than 2% of CD47 on (CD20−/CD47+) normal cells. See, Example 5. In other words entities described herein generally exhibit 95% or greater binding to (CD20+/CD47+) cells. Entities described herein exhibit 98% or greater binding to (CD20+/CD47+) cells.

The term “pharmaceutically acceptable” as used herein refers to approved by a regulatory agency of the Federal or a state government, or listed in the U.S. Pharmacopeia, European Pharmacopeia or other generally recognized pharmacopeia for use in animals, and more particularly in humans.

Concentrations, amounts, volumes, percentages and other numerical values may be presented herein in a range format. It is also to be understood that such range format is used merely for convenience and brevity and should be interpreted flexibly to include not only the numerical values explicitly recited as the limits of the range but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited.

Minor variations in the amino acid sequences of antibodies of the invention are contemplated as being encompassed by the present invention, providing that the variations in the amino acid sequence(s) maintain at least 75%, at least 80%, at least 90%, at least 95%, or at least 98 or 99% sequence homology or identity to the sequence of an antibody or antigen-binding fragment thereof provided herein.

Antibodies of the invention may include variants in which amino acid residues from one species are substituted for the corresponding residue in another species, either at the conserved or non-conserved positions. In one embodiment, amino acid residues at non-conserved positions are substituted with conservative or non-conservative residues. In particular, conservative amino acid replacements are contemplated.

As used herein, a “conservative amino acid substitution” refers to one in which the amino acid residue is replaced with an amino acid residue having a similar side chain. Families of amino acid residues having similar side chains have been defined in the art, including basic side chains (e.g., lysine, arginine, or histidine), acidic side chains (e.g., aspartic acid or glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, or cysteine), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, or tryptophan), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, or histidine). Thus, if an amino acid in a polypeptide is replaced with another amino acid from the same side chain family, the amino acid substitution is considered to be conservative. The inclusion of conservatively modified variants in an antibody of the invention does not exclude other forms of variant, for example polymorphic variants, interspecies homologs, and alleles.

As used herein, “non-conservative amino acid substitutions” include those in which (i) a residue having an electropositive side chain (e.g., arginine, histidine or lysine) is substituted for, or by, an electronegative residue (e.g., glutamate or aspartate), (ii) a hydrophilic residue (e.g., serine or threonine) is substituted for, or by, a hydrophobic residue (e.g., alanine, leucine, isoleucine, phenylalanine or valine), (iii) a cysteine or proline is substituted for, or by, any other residue, or (iv) a residue having a bulky hydrophobic or aromatic side chain (e.g., valine, histidine, isoleucine or tryptophan) is substituted for, or by, one having a smaller side chain (e.g., alanine or serine) or no side chain (e.g., glycine).

The terms “antibody” and “antibodies”, as used herein, refers to conventional isotypes and monospecific formats as well as multivalent antibodies including but not limited to current bispecific entity formats known in the art as well as bispecific antibodies including but not limited to formats otherwise described herein.

A typical antibody comprises at least two “light chains” (LC) and two “heavy chains” (HC). The light chains and heavy chains of such antibodies are polypeptides consisting of several domains. Each heavy chain comprises a heavy chain variable region (abbreviated herein as “VH”) and a heavy chain constant region (abbreviated herein as “CH”). The heavy chain constant region comprises the heavy chain constant domains CH1, CH2 and CH3 (antibody classes IgA, IgD, and IgG) and optionally the heavy chain constant domain CH4 (antibody classes IgE and IgM). Each light chain comprises a light chain variable domain (abbreviated herein as “VL”) and a light chain constant domain (abbreviated herein as “CL”). The variable regions VH and VL can be further subdivided into regions of hypervariability, termed complementarity determining regions (CDR), interspersed with regions that are more conserved, termed framework regions (FR). Each VH and VL is composed of three CDRs and four FRs, arranged from amino-terminus to carboxy-terminus in the following order: FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4. The “constant domains” of the heavy chain and of the light chain are not involved directly in binding of an antibody to a target, but exhibit various effector functions.

Binding between an antibody and its target antigen or epitope is mediated by the Complementarity Determining Regions (CDRs). The CDRs are regions of high sequence variability, located within the variable region of the antibody heavy chain and light chain, where they form the antigen-binding site. The CDRs are the main determinants of antigen specificity. Typically, the antibody heavy chain and light chain each comprise three CDRs which are arranged non-consecutively. The antibody heavy and light chain CDR3 regions play a particularly important role in the binding specificity/affinity of the antibodies according to the invention and therefore provide a further aspect of the invention.

Thus, the term “antigen binding fragment” as used herein incudes any naturally-occurring or artificially-constructed configuration of an antigen-binding polypeptide comprising one, two or three light chain CDRs, and/or one, two or three heavy chain CDRs, wherein the polypeptide is capable of binding to the antigen.

The sequence of a CDR may be identified by reference to any number system known in the art, for example, the Kabat system (Kabat, E. A., et al., Sequences of Proteins of Immunological Interest, 5th ed., Public Health Service, National Institutes of Health, Bethesda, Md. (1991); the Chothia system (Chothia &, Lesk, “Canonical Structures for the Hypervariable Regions of Immunoglobulins,” J. Mol. Biol. 196,901-917 (1987)); or the IMGT system (Lefranc et al., “IMGT Unique Numbering for Immunoglobulin and Cell Receptor Variable Domains and Ig superfamily V-like domains,” Dev. Comp. Immunol. 27,55-77 (2003)). CDRs shown herein employ the boundaries, i.e., size, according to KABAT. Position numbering of antibody constant regions described and referred to herein are generally according to KABAT. However, numbering of anti-CD47 VL and VH regions described herein, i.e., antibody residue positions and substituted positions, begins with the N-terminal residue of each variable region, i.e., VL or VH, particularly with reference to SEQ ID NO:325 and SEQ ID NO:326, respectively.

“Bispecific entities described herein” generally refers to the functionally defined antibodies, bispecific elemental formats, elemental sequences, antibodies, and antibody species described herein.

The term “Fab portion” or “arm”, as used herein, refers to an antigen-binding fragment of an antibody, i.e., a region of an antibody that binds an antigen. As used herein it comprises one variable domain of each of a light and heavy chain (VL/VH).

A “Fab′ fragment” contains a single light chain and a single heavy chain but in addition to the CH1 and the VH, a “Fab′ fragment” contains the region of the heavy chain between the CH1 and CH2 domains that is required for the formation of an inter-chain disulfide bond. Thus, two “Fab′ fragments” can associate via the formation of a disulphide bond to form a F(ab′)2 molecule.

A “F(ab′)2 fragment” contains two light chains and two heavy chains. Each chain includes a portion of the constant region necessary for the formation of an inter-chain disulfide bond between two heavy chains.

An “Fv fragment” contains only the variable regions of the heavy and light chain. It contains no constant regions.

A “single-domain antibody” is an antibody fragment containing a single antibody domain unit (e.g., VH or VL).

A “single-chain Fv” (“scFv”) is antibody fragment containing the VH and VL domain of an antibody, linked together to form a single chain. A polypeptide linker is commonly used to connect the VH and VL domains of the scFv.

A “tandem scFv”, also known as a TandAb®, is a single-chain Fv molecule formed by covalent bonding of two scFvs in a tandem orientation with a flexible peptide linker.

A “bi-specific T cell engager” (BiTE®) is a fusion protein consisting of two single-chain variable fragments (scFvs) on a single peptide chain. One of the scFvs binds to T cells via the CD3 receptor, and the other to a tumour cell antigen.

A “diabody” is a small bivalent and bispecific antibody fragment comprising a heavy (VH) chain variable domain connected to a light chain variable domain (VL) on the same polypeptide chain (VH-VL) connected by a peptide linker that is too short to allow pairing between the two domains on the same chain (Kipriyanov, Int. J. Cancer 77 (1998), 763-772). This forces pairing with the complementary domains of another chain and promotes the assembly of a dimeric molecule with two functional antigen binding sites.

A “DARPin” is a bispecific ankyrin repeat molecule. DARPins are derived from natural ankyrin proteins, which can be found in the human genome and are one of the most abundant types of binding proteins. A DARPin library module is defined by natural ankyrin repeat protein sequences, using 229 ankyrin repeats for the initial design and another 2200 for subsequent refinement. The modules serve as building blocks for the DARPin libraries. The library modules resemble human genome sequences. A DARPin is composed of 4 to 6 modules. Because each module is approx. 3.5 kDa, the size of an average DARPin is 16-21 kDa. Selection of binders is done by ribosome display, which is completely cell-free and is described in He M. and Taussig M J., Biochem Soc Trans. 2007, November; 35 (Pt 5):962-5.

The terms “tumor” and “tumor cell” as used herein broadly refers to cancer cells including but not limited to cells undergoing aberrant proliferation, hematological oncology conditions, hematological malignancies, lymphoproliferative disorders, B-cell disorders, B-cell malignancies, and B-cell lymphoma.

IgG1 or IgG1 1+1 heterodimer format, as used herein, fundamentally refers to a whole IgG1 antibody composed of (i) one heavy chain (HC) and one light chain (LC), on one side, from one source, i.e., anti-CD47; and, one heavy chain (HC) and one light chain (LC), on the other side, from another source, e.g., anti-CD20. See, e.g., FIG. 2 and FIG. 6.

CD47

The value of cancer immunotherapy targeting the CD47/SIRPα axis is well-established. See, e.g., Weiskopf, K., et al., Eur J Cancer. 2017 May; 76:100; Feng, M., et al., Nat Rev Cancer. 2019 October; 19(10):568-586. Anti-CD47 approaches in the clinic have been be limited by the need for combination therapy, the tissue sink in targeting CD47 with a high-affinity binder, immunogenicity, and the observed hematologic toxicity with some of the clinical molecules (anemia, neutropenia, and/or thrombocytopenia).

CD47, while upregulated on tumor cells, is also ubiquitously expressed on all cells, including, at relatively high levels, NK cells, RBCs, and platelets. Monospecific agents targeting CD47 therefore tend to exhibit poor pharmacokinetic properties due to target-mediated drug disposition (TMDD) and side effects, including anemia and thrombocytopenia. Target-mediated drug disposition (TMDD) is the phenomenon in which a drug binds with high affinity to its pharmacological target site (such as a receptor) to such an extent that this affects its pharmacokinetic characteristics. Anti-CD47 IgG4 mAbs are generally required to reduce toxicity. Single anti-CD47, e.g., IgG1, agent activity thus tends to be limited.

Russ, A., et al., Blood Rev. 2018 November; 32(6):480 described a specific well-characterized IgG4 anti-CD47 antibody (CC-90002). See, particularly, WO2013119714 (U.S. Pat. No. 9,045,541). Various amino acid substitutions in this antibody, designed to increase cell-free production and reduce immunogenicity, have been described. See WO2016109415 (US20170369572); WO2018009499 (US20190241654); and WO2018183182. CC-90002 is a high affinity IgG4 PIE anti-CD47 molecule that binds to CD47 expressed on disease and normal tissues.

Because CD47 is expressed widely on normal tissues as well as on tumor cells, however, a high-affinity anti-CD47 antibody may lead to undesirable toxicity. Provided herein, therefore, are bispecific antibodies comprising a CD47-binding domain that improves upon CC-90002 with respect to toxicity and efficacy. In particular, the bispecific entities described herein selectively and safely target tumor cells, with little to no binding to CD47 in peripheral tissues. The present invention is directed to an antibody comprising at least one Fab portion that binds CD47 and at least one Fab portion that binds CD20; wherein the Fab portion that binds CD47 exhibits low affinity for CD47 (e.g., Kd greater than 100 nM); and, wherein the Fab portion that binds CD20 exhibits high affinity for CD20 (e.g., Kd less than 5 nM); and, wherein the bispecific antibody selectively binds CD47 in tumor cells and is substantially free of binding to CD47 in normal cells.

CC-90002 is provided as a reference parental sequence and as a source of anti-CD47 elements for construction of some of the bispecific entities described herein. CC-90002 VL CDRs are SEQ ID NO:347 (CDRL1), SEQ ID NO:348 (CDRL2), and SEQ ID NO:349 (CDRL3). CC-90002 VH CDRs are SEQ ID NO:350 (CDRH1), SEQ ID NO:351 (CDRH2), and SEQ ID NO:352 (CDRH3). CC-90002 VL (SEQ ID NO:325) and VH (SEQ ID NO:326) are also provided for reference. CC-90002 VL fused to a native IgG1 LC constant region to form a whole LC for reference is provided as CC-90002 WHOLE LC/IgG1 (SEQ ID NO:327). CC-90002 VH fused to a native IgG1 HC constant region to form a whole HC for reference is provided as CC-90002 whole HC/IgG1 (SEQ ID NO:328).

Both VH and VL regions of CC-90002 were engineered to reduce immunogenicity, while retaining functionality for employment in bispecific entities described herein.

Bispecific entities described and exemplified herein, for example, are demonstrated to overcome the challenges of single agent anti-CD47 mAb therapy. Due to the detuned affinity for CD47, CD47×CD20 bispecific entities described and provided herein bind preferentially to CD20⁺ Tumor Associated Antigen (TAA) cells, thereby reducing the sink effect mediated by CD47⁺ cells and on-target off-tumor toxicity. Together, the cellular potency, in vivo efficacy, and safety data indicate that CD47×CD20 bispecifics described and exemplified herein offer a unique option as single agents for CD20-positive B cell malignancy, for example.

FIG. 1 is a schematic illustration of certain attributes of bispecific entities described herein engineered to overcome the challenge of ubiquitous CD47 expression including low affinity binding without avidity to CD47; minimal binding to normal cells, i.e., no tissue sink; high affinity selective avidity binding to the Tumor Associated Antigen (TAA) CD20; which results in selective binding to tumor cells.

CD47×CD20 bispecifics provided herein may comprise a CD20 binding domain from any high-affinity CD20 binder. Rituximab LC (SEQ ID NO:329) and HC (SEQ ID NO:330) are preferred sources of anti-CD20 elements for construction of bispecific entities described herein. In certain embodiments, the bispecific antibodies provided herein comprise one or both of the rituximab VL (SEQ ID NO:323) and VH (SEQ ID NO:324), or comprise Rituximab VL CDRs: SEQ ID NO:353 (CDRL1), SEQ ID NO:354 (CDRL2), and SEQ ID NO:355 (CDRL3); and, Rituximab VH CDRs: SEQ ID NO:356 (CDRH1), SEQ ID NO:357 (CDRH2), and SEQ ID NO:358 (CDRH3), respectively. Anti-CD20 IgG1 LC and HC constant regions as otherwise described herein are fused to the carboxy termini of rituximab VL (SEQ ID NO:323) and rituximab VH (SEQ ID NO:324), respectively. Anti-CD20 LC (SEQ ID NO:331) is preferred for employment in construction of bispecific entities of the present invention. Anti-CD20 HC (SEQ ID NO:332) is preferred for employment in construction of bispecific entities of the present invention.

Example bispecific entities described herein selectively and safely target CD20⁺ tumor cells, with substantially no of binding to CD47 in peripheral tissues, RBCs, and platelets, providing prolonged half-life with lower toxicity and wherein the antibody mediates complement-dependent cytotoxicity (CDC) of the tumor cells.

Bispecific Entities are Preferably of the IgG1 1+1 Heterodimer Format.

In certain embodiments, the bispecific antibodies provided herein comprise two antigen binding arms, which are covalently connected to form a single entity. IgG bispecific antibodies that employ two Fab domains require careful consideration with regards to expression and purification strategy to ensure proper assembly of the desired product. Efforts can be taken at the genetic level to bias the expression of the desired bispecific antibody. For instance, substitutions in the CH3 domains of the IgG Fc to drive heterodimerization of the Fc have been described. Further, knob-in hole strategy utilizes steric hindrance to create complementary asymmetric molecular faces between two different Fc CH3 domains. Other strategies known in the art employ electrostatic complementarity to drive specificity. Alternatively, wild-type IgG scaffolds can be used and the resulting combination of products can be separated during to protein purification to isolate the desired product.

Preferred bispecific antibodies of the present invention are fundamentally native human IgG1 antibodies composed of, (A) one anti-CD47 IgG1 (monomeric) portion which contains one entire light chain (LC) and one entire heavy chain (HC), as well as (B) one anti-CD20 IgG1 (monomeric) portion which contains one entire light chain (LC) and one entire heavy chain (HC). The two monomers form a conventional dimeric IgG1 antibody wherein one arm (Fab′) provides for attenuated binding of CD47 while the other arm (Fab₂) provides for affinity binding and avidity for CD20. FIG. 2 and FIG. 6 illustrate CD47×CD20 example architecture described herein and example protein engineering features.

Preferred monomeric elements of the IgG1 1+1 heterodimers described herein each contain certain subsequences within the LC and HC constant regions that reduce homodimer formation during production of the IgG1 1+1 heterodimer format. In one embodiment, an anti-CD47 LC constant region that ensures proper LC/HC pairing during production comprises SEQ ID NO:340. In another embodiment, an anti-CD47 HC constant region that ensures Fc heterodimer formation during production comprise SEQ ID NO:342. Preferred anti-CD20 LC constant region to ensure proper LC/HC pairing during production comprise SEQ ID NO:344. Preferred anti-CD20 HC constant region to ensure Fc heterodimer formation during production comprise SEQ ID NO:346. An example anti-CD47 LC constant region to ensure proper LC/HC pairing during production is SEQ ID NO:339. An example anti-CD47 HC constant region to ensure Fc heterodimer formation during production is SEQ ID NO:341. An example anti-CD20 LC constant region to ensure proper LC/HC pairing during production is SEQ ID NO:343. An example anti-CD20 HC constant region to ensure Fc heterodimer formation during production is SEQ ID NO:345.

Preferred IgG1 constant regions for employment with 161 Fabs described herein in IgG1 1+1 heterodimer format wherein the Fabs provide for attenuated binding of CD47 are LC constant region SEQ ID NO:339 and HC constant region SEQ ID NO:341.

Provided is an anti-CD47 IgG1 LC Constant Region comprising substitutions Q124E, L135W, Q160E, and T180E ensure proper LC/HC pairing during production of the IgG1 1+1 heterodimer format, as compared to CC-90002.

Further provided herein is a preferred anti-CD47 IgG1 LC Constant Region (SEQ ID NO:339). In certain embodiments, e.g., certain embodiments of the bispecific antibodies provided herein, an anti-CD47 VL region provided herein is fused to the amino terminus of SEQ ID NO:339. SEQ ID NO:340 is internal to SEQ ID NO:339. SEQ ID NO: 339 and SEQ ID NO: 440 comprise substitutions Q124E, L135W, Q160E, and T180E, that ensure proper LC/HC pairing during production of the IgG1 1+1 heterodimer format.

Provided is an anti-CD47 IgG1 HC Constant Region comprising substitutions Q179K, T371V, T389L, K420L, and T422W to ensure proper LC/HC pairing and Fc heterodimer formation during production of the IgG1 1+1 heterodimer format.

Further provided herein is a preferred anti-CD47 IgG1 HC Constant Region (SEQ ID NO:341). In certain embodiments, e.g., certain embodiments of the bispecific antibodies provided herein, an anti-CD47 VH region provided herein is fused to the amino terminus of SEQ ID NO:341. SEQ ID NO:342 is internal to SEQ ID NO:341. SEQ ID NO: 341 and SEQ ID NO: 342 comprise substitutions Q179K, T371V, T389L, K420L, and T422W to ensure Fc heterodimer formation during production of the IgG1 1+1 heterodimer format.

Provided is an anti-CD20 IgG1 LC Constant Region comprising substitutions F116A, Q124R, L135V, T178R that ensure proper LC/HC pairing during production of the IgG1 1+1 heterodimer format, as compared to rituximab.

Further provided herein is a preferred anti-CD20 IgG1 LC Constant Region (SEQ ID NO:343). In certain embodiments, e.g., certain embodiments of the bispecific antibodies provided herein, an anti-CD20 VL region provided herein is fused to the amino terminus of SEQ ID NO:343. SEQ ID NO:344 is internal to SEQ ID NO:343. SEQ ID NO:343 and SEQ ID NO:344 comprise substitutions F116A, Q124R, L135V, and T178R that reduce homodimer formation during production of the IgG1 1+1 heterodimer format.

Provided is an anti-CD20 IgG1 HC Constant Region comprising substitutions A139W, L143E, K145T, Q179E, T371V, L372Y, F436A, and Y438V that ensure Fc heterodimer formation during production of the IgG1 1+1 heterodimer format, as compared to rituximab.

Further provided herein is a preferred anti-CD20 IgG1 HC Constant Region (SEQ ID NO:345). In certain embodiments, e.g., certain embodiments of the bispecific antibodies provided herein, an anti-CD20 VH region provided herein is fused to the amino terminus of SEQ ID NO:345. SEQ ID NO:346 is internal to SEQ ID NO:345. SEQ ID NO:345 and SEQ ID NO:346 comprise substitutions A139W, L143E, K145T, Q179E, T371V, L372Y, F436A, and Y438V that reduce homodimer formation during production of the IgG1 1+1 heterodimer format.

CD47×CD20 Bispecifics

A CD47×CD20 bispecific program was initiated to identify therapeutic antibodies that are able to block human CD47 binding to SIRPα only on CD20 expressing cells. Examples resulting from that project and provided herein bind with high affinity to CD20 while exhibiting a detuned affinity to CD47. Once bound to CD20 on tumor cells the antibodies potently block CD47-SIRPα interaction and co-engage activating receptors FcγRs on effector cells through IgG1 Fc, resulting in activation of macrophage mediated phagocytosis and natural killer (NK) cell mediated cytotoxicity against tumor cells.

Bispecific Antibodies Comprising Anti-CD47 Derived from CC-90002

CD47 Epitope Mapping and CC-90002

The anti-CD47 epitope was determined by solving the crystal structure of a non-detuned parental version of CC-90002 (408_437) Fab (VL: SEQ ID NO:387; VH: SEQ ID NO:388) in complex with the human CD47 extracellular domain at 2.4 A resolution. All three light chain (LC) CDRs (SEQ ID NO:347, SEQ ID NO:348, SEQ ID NO:349) and the heavy chain (HC) CDR2 (SEQ ID NO:351) and HC CDR3 (SEQ ID NO:352) participate in binding to a large surface area of the CD47 ECD. The HC CDRs make multiple contacts to the KGRD loop of CD47 and the LC CDRs overlap with the SIRPα binding site, which explains the ability of CC-90002 and bispecific entities described herein to block SIRPα binding.

CD47×CD20 bispecific entities described herein are designed to promote CD20-restricted blockade of the CD47-SIRPα “don't eat me” signal on cancer cells that express both CD20 and CD47, while sparing CD47⁺/CD20⁻ normal cells. Multiple steps of protein engineering led to the anti-CD47 Fabs of the bispecific entities described herein. (1) Protein engineering was employed on both VH and VL chains of CC-90002 to reduce immunogenicity, while retaining functionality; and, (2) Protein engineering was also employed to detune CC-90002. IgG1 bispecific antibodies targeting CD47 and CD20 with reduced affinity to CD47, described and exemplified herein, 1) retain efficacy in mediating anti-tumor function by targeting the CD47-SIRPα interaction and engaging activating receptors FcγRs; 2) minimize target-mediated sink effects and toxicity observed with anti-CD47 therapeutics; 3) incorporate CD47 and CD20 engagement in a single molecule avoiding the need for combination therapy with 2 monoclonal antibodies.

Protein Design

A crystal structure of the effector antigen CD47 was bound to a high affinity anti-CD47 Fab (CC-90002 (408_437 VL: SEQ ID NO:899; 408_437 VH: SEQ ID NO:900)) to guide the construction of an in silico library of Fab variants predicted to have a range of lower affinities, good stability, and low immunogenicity. Variants from this library were expressed as IgG1 bispecifics with a high affinity anti-CD20 Fab (rituximab (VL: SEQ ID NO:323; VH: SEQ ID NO:324)).

The resulting 143 physical constructs were screened for selectivity and potency using cell-based assays for CD47 binding and SIRPα blocking to identify those variants that effectively bound to the effector antigen, CD47, on target cells co-expressing the selectivity antigen, CD20, but which bound minimally to a non-target cell line that expressed only the effector antigen, CD47.

Example anti-CD47 whole LC and HC, LC and HC constant regions, VL and VH regions, and CDR sequences are provided and otherwise described herein that have substantially reduced binding affinity for CD47 and reduced immunogenicity as compared to CC-90002, including but not limited to the IgG1 isotype. IgG1 1+1 heterodimer format is preferred, as described infra, comprising (A) one anti-CD47 IgG1 (monomeric) portion which contains one entire light chain (LC) and one entire heavy chain (HC), as well as (B) one anti-CD20 IgG1 (monomeric) portion which contains one entire light chain (LC) and one entire heavy chain (HC).

Antibodies of the present invention comprise VL and VH amino acid sequences derived from CC-90002, i.e., SEQ ID NO:325 and SEQ ID NO:326, respectively, wherein the binding affinity for CD47 is substantially attenuated, i.e., Fab portion that binds CD47 exhibits low affinity. A range of affinities to CD47 from the screen of detuned anti-CD47 binders described herein were found to have dramatically reduced binding to non-target cells and yet were still able to effectively bind to CD47 in an avid manner when recruited to the surface of the target cell after binding to CD20. Initial detuned CD47×CD20 bispecific leads achieved this selectivity with affinities that ranged from about 0.5 μM to about 2.5 μM. FIGS. 3A-3C. TPP-1360, for example, was measured to have an affinity for human CD47 ECD of 1.7 μM Kd, which reflects about 350× decrease in affinity relative to the parental anti-CD47 binder. TPP-1362 was measured to have an affinity for human CD47 ECD of 0.796 μM Kd, which reflects ˜150× decrease in affinity relative to the parental anti-CD47 binder. Detuned CD47×CD20 bispecific entitled described herein exhibit selectivity with affinities that range from about 0.2 μM to about 4 μM.

Bispecific entities described herein selectively bind CD47 on CD20 expressing tumor cells and are substantially free of binding to CD47 in normal cells. The ratio of binding to Raji (CD47+CD20+) vs human RBC in the co-culture binding assay for bispecific entities described herein is about 6,000 fold, for example. The ratio of binding to human B cells (CD47+CD20+) vs human RBC for bispecific entities described herein is about 700 fold, for example. The level of selection of bispecific entities described herein exhibit selection in the range from about 400 to about 8,000 fold depending upon the expression level of CD20 and CD47 on tumor cells and normal cells. Accordingly, assuming a fixed level of CD47 expression, as CD20 levels increase bispecific entitled described herein exhibit increased selectivity and potency.

Example antibodies of the present invention also comprise VL and VH regions derived from CC-90002, i.e., SEQ ID NO:325 and SEQ ID NO:326, respectively, wherein the VL, VH, or both comprise one or more amino acid substitutions that substantially reduce the immunogenicity of the resulting antibody. Example antibodies of the present invention comprise VL and VH regions derived from CC-90002, SEQ ID NO:325 and SEQ ID NO:326, respectively, wherein the VL, VH, or both sequences comprise one or more amino acid substitutions that reduce the binding affinity of the resulting antibody for CD47 and substantially reduced the immunogenicity of the resulting antibody.

Accordingly, preferred antibodies derived from CC-90002 described herein exhibit 1-7 amino acid substitutions relative to VL SEQ ID NO:325; and, 141 amino acid substitutions relative to VH SEQ ID NO:326.

Further contemplated and otherwise functionally described herein are antibodies derived from CC-90002 that exhibit 8 amino acid substitutions relative to VL SEQ ID NO:325. Further contemplated and otherwise functionally described herein are antibodies derived from CC-90002 that exhibit 9 amino acid substitutions relative to VL SEQ ID NO:325. Further contemplated and otherwise functionally described herein are antibodies derived from CC-90002 that exhibit 10 amino acid substitutions relative to VL SEQ ID NO:325.

Further contemplated and otherwise functionally described herein are antibodies derived from CC-90002 that exhibit 12 amino acid substitutions relative to VH SEQ ID NO:326. Further contemplated and otherwise functionally described herein are antibodies derived from CC-90002 that exhibit 13 amino acid substitutions relative to VH SEQ ID NO:326. Further contemplated and otherwise functionally described herein are antibodies derived from CC-90002 that exhibit 14 amino acid substitutions relative to VH SEQ ID NO:326.

Provided herein is a CD47 antibody wherein the anti-CD47 VL exhibits 1-7 amino acid substitutions relative to SEQ ID NO:325 wherein at least one (1) of said amino acid substitutions is selected from the group consisting of A10S, M11L, K24R, A51E, N52S, L54F, and S56D; and the anti-CD47 VH exhibits 1-11 amino acid substitutions relative to SEQ ID NO:326 wherein at least one (1) of said amino acid substitutions is selected from the group consisting of T14P, 043K, A44G, E59Y, D66G, M76T, S84R, S88A, M93V, S102E, and T115L.

Also provided herein is a CD47 antibody described herein wherein the anti-CD47 VL exhibits at least one (1), at least two (2), at least three (3), at least four (4), at least five (5), at least six (6) or at least seven (7) amino acid substitutions relative to SEQ ID NO:325 wherein the amino acid substitution is selected from the group consisting of A10S, M11L, K24R, A51E, N52S, L54F, and S56D.

The invention is directed to an antibody described herein wherein the anti-CD47 VL exhibits at least seven (7) amino acid substitutions relative to SEQ ID NO:325 wherein seven (7) of the amino acid substitutions are A10S, M11L, K24R, A51E, N52S, L54F, and S56D.

The invention is directed to an antibody described herein wherein the anti-CD47 VH exhibits at least one (1), two (2), three (3), four (4), five (5), six (6), seven (7), eight (8), nine (9), ten (10), or eleven (11) amino acid substitution relative to SEQ ID NO:326 wherein the amino acid substitution is selected from the group consisting of T14P, 043K, A44G, E59Y, D66G, M76T, S84R, S88A, M93V, S102E, and T115L.

The invention is directed to an antibody described herein wherein the anti-CD47 VH exhibits at least eleven (11) amino acid substitutions relative to SEQ ID NO:326 wherein eleven (11) of the amino acid substitutions are T14P, Q43K, A44G, E59Y, D66G, M76T, S84R, S88A, M93V, 5102E, and T115L.

Anti-CD47 LC (SEQ ID NO:335) and HC (SEQ ID NO:336) are preferred sources of anti-CD47 elements for construction of bispecific entities described herein, particularly VL (SEQ ID NO:319) and VH (SEQ ID NO:320) which comprise VL CDRs SEQ ID NO:365 (CDRL1), SEQ ID NO:366 (CDRL2), and SEQ ID NO:367 (CDRL3); and, VH CDRs SEQ ID NO:368 (CDRH1), SEQ ID NO:369 (CDRH2), and SEQ ID NO:370 (CDRH3), respectively. Substitutions A10S, M11L, K24R, A51E, N52S, L54F, and S56D are important VL (SEQ ID NO:319) substitutions with regard to CC-90002 to effect low CD47 binding affinity and reduce immunogenicity. T14P, Q43K, A44G, E59Y, D66G, M76T, S84R, S88A, M93V, S102E, and T115L are important VH (SEQ ID NO:320) with regard to CC-90002 to effect low CD47 binding affinity (particularly E59Y and S102E) and reduce immunogenicity. Anti-CD47 IgG1 LC and HC Constant Regions as otherwise described herein, e.g., SEQ ID NO:339 and SEQ ID NO:341, respectively, are in certain embodiments fused to the carboxy termini of VL (SEQ ID NO:319) and VH (SEQ ID NO:320). Anti-CD47 LC (SEQ ID NO:335) is preferred for employment in construction of bispecific entities of the present invention. Anti-CD47 HC (SEQ ID NO:336) is preferred for employment in construction of bispecific entities of the present invention. Substitutions Q124E, L135W, Q160E, and T180E are important SEQ ID NO:335 positions to ensure proper LC/HC pairing formation during production of the IgG1 1+1 heterodimer format. Substitutions Q179K, T371V, T389L, K420L, and T422W are important SEQ ID NO:336 positions to reduce propensity for homodimer formation during production of the IgG1 1+1 heterodimer format.

The invention is further particularly directed to an antibody otherwise described herein wherein the anti-CD47 VL exhibits 1-3 amino acid substitutions relative to SEQ ID NO:325 wherein at least one (1), at least two (2), or at least three (3) amino acid substitution in the anti-CD47 VL (SEQ ID NO: 325) are selected from the group consisting of A10S, M11L, and K24R (e.g., SEQ ID NO:321); and, the anti-CD47 VH exhibits 1-11 amino acid substitutions relative to SEQ ID NO:326 wherein at least one (1), at least two (2), at least three (3), at least four (4), at least five (5), at least six (6), at least seven (7), at least eight (8), at least nine (9), at least ten (10) or at least eleven (11) amino acid substitution in the anti-CD47 VH (SEQ ID NO: 326) are selected from the group consisting of T14P, Q43K, A44G, E59Y, D66G, M76T, S84R, S88A, M93V, S102E, and T115L (e.g., SEQ ID NO:322).

The invention is particularly directed to an antibody otherwise described herein wherein the anti-CD47 VH exhibits 1-11 amino acid substitutions relative to SEQ ID NO:326 wherein at least one (1), at least two (2), at least three (3), at least four (4), at least five (5), at least six (6), at least seven (7), at least eight (8), at least nine (9), at least ten (10) or at least eleven (11) amino acid substitution in the anti-CD47 VH (SEQ ID NO: 326) are selected from the group consisting of T14P, Q43K, A44G, E59Y, D66G, M76T, S84R, S88A, M93V, S102E, and T115L (e.g., SEQ ID NO:322).

Anti-CD47 LC (SEQ ID NO:337) and HC (SEQ ID NO:338) are preferred sources of anti-CD47 elements for construction of bispecific entities described herein, particularly VL (SEQ ID NO:321) and VH (SEQ ID NO:322) which comprise VL CDRs SEQ ID NO:371, SEQ ID NO:372, and SEQ ID NO:373; and, VH CDRs SEQ ID NO:374, SEQ ID NO:375, and SEQ ID NO:376, respectively. A10S, M11L, and K24R are important VL (SEQ ID NO:321) positions to effect low CD47 binding affinity and reduce immunogenicity. Substitutions T14P, Q43K, A44G, E59Y, D66G, M76T, S84R, S88A, M93V, S102E, and T115L are important VH (SEQ ID NO:322) positions to effect low CD47 binding affinity (particularly E59Y and S102E) and reduce immunogenicity. Anti-CD47 IgG1 LC and HC Constant Regions as otherwise described herein, e.g., SEQ ID NO:339 and SEQ ID NO:341, respectively, are fused to the carboxy termini of VL (SEQ ID NO:321) and VH (SEQ ID NO:322). Anti-CD47 LC (SEQ ID NO:337) is preferred for employment in construction of bispecific entities of the present invention. Anti-CD47 HC (SEQ ID NO:338) is preferred for employment in construction of bispecific entities of the present invention. Substitutions Q124E, L135W, Q160E, and T180E are important SEQ ID NO:337 positions for reducing the propensity for homodimer formation during production of the IgG1 1+1 heterodimer format. Substitutions Q179K, T371V, T389L, K420L, and T422W are important SEQ ID NO:338 positions for reducing the propensity for homodimer formation during production of the IgG1 1+1 heterodimer format.

The invention is particularly directed to an antibody otherwise described herein wherein the anti-CD47 VL exhibits 1-10 amino acid substitutions relative to SEQ ID NO:325 wherein at least one (1), at least two (2), at least three (3), at least four (4 at least five (5), at least six (6), at least seven (7), at least eight (8), at least nine (9), or at least ten (10) amino acid substitution in the anti-CD47 VL (SEQ ID NO: 325) are selected from the group consisting of A10S, M11L, K24Q, K39D, K42T, K45Q, A51E, N52S, L54F, and S56D (e.g., SEQ ID NO:317); and, the anti-CD47 VH exhibits 1-11 amino acid substitutions relative to SEQ ID NO:326 wherein at least one (1), at least two (2), at least three (3), at least four (4), at least five (5), at least six (6), at least seven (7), at least eight (8), at least nine (9), at least ten (10) or at least eleven (11) amino acid substitution in the anti-CD47 VH (SEQ ID NO: 326) are selected from the group consisting of T14P, A44G, E59Y, D66G, M76T, S84A, R87T, 588A, M93V, 5102E, and T115L (e.g., SEQ ID NO:318).

The invention is particularly directed to an antibody otherwise described herein wherein the anti-CD47 VH exhibits 1-11 amino acid substitutions relative to SEQ ID NO:326 wherein at least one (1), at least two (2), at least three (3), at least four (4), at least five (5), at least six (6), at least seven (7), at least eight (8), at least nine (9), at least ten (10) or at least eleven (11) amino acid substitutions in the anti-CD47 VH (SEQ ID NO: 326) are selected from the group consisting of T14P, A44G, E59Y, D66G, M76T, S84A, R87T, S88A, M93V, S102E, and T115L (e.g., SEQ ID NO:318).

Anti-CD47 LC (SEQ ID NO:333) and HC (SEQ ID NO:334) are preferred sources of anti-CD47 elements for construction of bispecific entities described herein, particularly VL (SEQ ID NO:317) and VH (SEQ ID NO:318) which comprise VL CDRs: SEQ ID NO:359, SEQ ID NO:360, and SEQ ID NO:361; and, VH CDRs: SEQ ID NO:362, SEQ ID NO:363, and SEQ ID NO:364, respectively. Substitutions A10S, M11L, K24Q, K39D, K42T, K45Q, A51E, N52S, L54F, and S56D are important VL (SEQ ID NO:317) positions to effect low CD47 binding affinity and reduce immunogenicity. Substitutions T14P, A44G, E59Y, D66G, M76T, 584A, R87T, S88A, M93V, 5102E, and T115L are important VH (SEQ ID NO:318) positions to effect low CD47 binding affinity (particularly E59Y and 5102E) and reduce immunogenicity. Anti-CD47 IgG1 LC and HC Constant Regions as otherwise described herein, e.g., SEQ ID NO:339 and SEQ ID NO:341, respectively, are fused to the carboxy termini of VL (SEQ ID NO:317) and VH (SEQ ID NO:318). Anti-CD47 LC (SEQ ID NO:333) is preferred for employment in construction of bispecific entities of the present invention. Anti-CD47 HC (SEQ ID NO:334) is preferred for employment in construction of bispecific entities of the present invention. Substitutions Q124E, L135W, Q160E, and T180E are important SEQ ID NO:333 positions to reduce propensity for homodimer formation during production of the IgG1 1+1 heterodimer format. Substitutions Q179K, T371V, T389L, K420L, and T422W are important SEQ ID NO:334 positions for reducing the propensity for homodimer formation during production of the IgG1 1+1 heterodimer format.

Example antibodies described and contemplated herein comprise anti-CD20 VL CDRs RASSSVSYIH (SEQ ID NO:353), ATSNLAS (SEQ ID NO:354), and QQWTSNPPT (SEQ ID NO:355); and, VH CDRs SYNMH (SEQ ID NO:356), AIYPGNGDTSYNQKFKG (SEQ ID NO:357), and STYYGGDWYFNV (SEQ ID NO:358). Example bispecific antibodies otherwise described herein comprise anti-CD20 VL (SEQ ID NO: 323) and VH (SEQ ID NO: 324). Example preferred species bispecific antibodies functionally described herein comprise anti-CD20 LC (SEQ ID NO:331) and anti-CD20 HC (SEQ ID NO:332).

161 Examples of Detuned Anti-CD47 VL/VH Fabs Derived from CC-90002

Further provided herein are 161 VL and VH Fabs derived from parental antibody CC-90002. For each of the 161 Fabs, the VL amino acid sequences are provided as odd SEQ ID Nos 1-321; and the VH amino acid sequences are provided as even SEQ ID Nos 2-322. Identified Fabs (VL/VH pairs) identified are each numbered as adjacent SEQ ID NOs, i.e., pairs disclosed herein following the pattern: SEQ ID NO:1/SEQ ID NO:2; SEQ ID NO:3/SEQ ID NO:4, and so forth to SEQ ID NO:321/SEQ ID NO:322:

SEQ ID NO:1/SEQ ID NO:2; SEQ ID NO:3/SEQ ID NO:4; SEQ ID NO:5/SEQ ID NO:6; SEQ ID NO:7/SEQ ID NO:8; SEQ ID NO:9/SEQ ID NO:10; SEQ ID NO:11/SEQ ID NO:12; SEQ ID NO:13/SEQ ID NO:14; SEQ ID NO:15/SEQ ID NO:16; SEQ ID NO:17/SEQ ID NO:18; SEQ ID NO:19/SEQ ID NO:20; SEQ ID NO:21/SEQ ID NO:22; SEQ ID NO:23/SEQ ID NO:24; SEQ ID NO:25/SEQ ID NO:26; SEQ ID NO:27/SEQ ID NO:28; SEQ ID NO:29/SEQ ID NO:30; SEQ ID NO:31/SEQ ID NO:32; SEQ ID NO:33/SEQ ID NO:34; SEQ ID NO:35/SEQ ID NO:36; SEQ ID NO:37/SEQ ID NO:38; SEQ ID NO:39/SEQ ID NO:40; SEQ ID NO:41/SEQ ID NO:42; SEQ ID NO:43/SEQ ID NO:44; SEQ ID NO:45/SEQ ID NO:46; SEQ ID NO:47/SEQ ID NO:48; SEQ ID NO:49/SEQ ID NO:50; SEQ ID NO:51/SEQ ID NO:52; SEQ ID NO:53/SEQ ID NO:54; SEQ ID NO:55/SEQ ID NO:56; SEQ ID NO:57/SEQ ID NO:58; SEQ ID NO:59/SEQ ID NO:60; SEQ ID NO:61/SEQ ID NO:62; SEQ ID NO:63/SEQ ID NO:64; SEQ ID NO:65/SEQ ID NO:66; SEQ ID NO:67/SEQ ID NO:68; SEQ ID NO:69/SEQ ID NO:70; SEQ ID NO:71/SEQ ID NO:72; SEQ ID NO:73/SEQ ID NO:74; SEQ ID NO:75/SEQ ID NO:76; SEQ ID NO:77/SEQ ID NO:78; SEQ ID NO:79/SEQ ID NO:80; SEQ ID NO:81/SEQ ID NO:82; SEQ ID NO:83/SEQ ID NO:84; SEQ ID NO:85/SEQ ID NO:86; SEQ ID NO:87/SEQ ID NO:88; SEQ ID NO:89/SEQ ID NO:90; SEQ ID NO:91/SEQ ID NO:92; SEQ ID NO:93/SEQ ID NO:94; SEQ ID NO:95/SEQ ID NO:96; SEQ ID NO:97/SEQ ID NO:98; SEQ ID NO:99/SEQ ID NO:100; SEQ ID NO:101/SEQ ID NO:102; SEQ ID NO:103/SEQ ID NO:104; SEQ ID NO:105/SEQ ID NO:106; SEQ ID NO:107/SEQ ID NO:108; SEQ ID NO:109/SEQ ID NO:110; SEQ ID NO:111/SEQ ID NO:112; SEQ ID NO:113/SEQ ID NO:114; SEQ ID NO:115/SEQ ID NO:116; SEQ ID NO:117/SEQ ID NO:118; SEQ ID NO:119/SEQ ID NO:120; SEQ ID NO:121/SEQ ID NO:122; SEQ ID NO:123/SEQ ID NO:124; SEQ ID NO:125/SEQ ID NO:126; SEQ ID NO:127/SEQ ID NO:128; SEQ ID NO:129/SEQ ID NO:130; SEQ ID NO:131/SEQ ID NO:132; SEQ ID NO:133/SEQ ID NO:134; SEQ ID NO:135/SEQ ID NO:136; SEQ ID NO:137/SEQ ID NO:138; SEQ ID NO:139/SEQ ID NO:140; SEQ ID NO:141/SEQ ID NO:142; SEQ ID NO:143/SEQ ID NO:144; SEQ ID NO:145/SEQ ID NO:146; SEQ ID NO:147/SEQ ID NO:148; SEQ ID NO:149/SEQ ID NO:150; SEQ ID NO:151/SEQ ID NO:152; SEQ ID NO:153/SEQ ID NO:154; SEQ ID NO:155/SEQ ID NO:156; SEQ ID NO:157/SEQ ID NO:158; SEQ ID NO:159/SEQ ID NO:160; SEQ ID NO:161/SEQ ID NO:162; SEQ ID NO:163/SEQ ID NO:164; SEQ ID NO:165/SEQ ID NO:166; SEQ ID NO:167/SEQ ID NO:168; SEQ ID NO:169/SEQ ID NO:170; SEQ ID NO:171/SEQ ID NO:172; SEQ ID NO:173/SEQ ID NO:174; SEQ ID NO:175/SEQ ID NO:176; SEQ ID NO:177/SEQ ID NO:178; SEQ ID NO:179/SEQ ID NO:180; SEQ ID NO:181/SEQ ID NO:182; SEQ ID NO:183/SEQ ID NO:184; SEQ ID NO:185/SEQ ID NO:186; SEQ ID NO:187/SEQ ID NO:188; SEQ ID NO:189/SEQ ID NO:190; SEQ ID NO:191/SEQ ID NO:192; SEQ ID NO:193/SEQ ID NO:194; SEQ ID NO:195/SEQ ID NO:196; SEQ ID NO:197/SEQ ID NO:198; SEQ ID NO:199/SEQ ID NO:200; SEQ ID NO:201/SEQ ID NO:202; SEQ ID NO:203/SEQ ID NO:204; SEQ ID NO:205/SEQ ID NO:206; SEQ ID NO:207/SEQ ID NO:208; SEQ ID NO:209/SEQ ID NO:210; SEQ ID NO:211/SEQ ID NO:212; SEQ ID NO:213/SEQ ID NO:214; SEQ ID NO:215/SEQ ID NO:216; SEQ ID NO:217/SEQ ID NO:218; SEQ ID NO:219/SEQ ID NO:220; SEQ ID NO:221/SEQ ID NO:222; SEQ ID NO:223/SEQ ID NO:224; SEQ ID NO:225/SEQ ID NO:226; SEQ ID NO:227/SEQ ID NO:228; SEQ ID NO:229/SEQ ID NO:230; SEQ ID NO:231/SEQ ID NO:232; SEQ ID NO:233/SEQ ID NO:234; SEQ ID NO:235/SEQ ID NO:236; SEQ ID NO:237/SEQ ID NO:238; SEQ ID NO:239/SEQ ID NO:240; SEQ ID NO:241/SEQ ID NO:242; SEQ ID NO:243/SEQ ID NO:244; SEQ ID NO:245/SEQ ID NO:246; SEQ ID NO:247/SEQ ID NO:248; SEQ ID NO:249/SEQ ID NO:250; SEQ ID NO:251/SEQ ID NO:252; SEQ ID NO:253/SEQ ID NO:254; SEQ ID NO:255/SEQ ID NO:256; SEQ ID NO:257/SEQ ID NO:258; SEQ ID NO:259/SEQ ID NO:260; SEQ ID NO:261/SEQ ID NO:262; SEQ ID NO:263/SEQ ID NO:264; SEQ ID NO:265/SEQ ID NO:266; SEQ ID NO:267/SEQ ID NO:268; SEQ ID NO:269/SEQ ID NO:270; SEQ ID NO:271/SEQ ID NO:272; SEQ ID NO:273/SEQ ID NO:274; SEQ ID NO:275/SEQ ID NO:276; SEQ ID NO:277/SEQ ID NO:278; SEQ ID NO:279/SEQ ID NO:280; SEQ ID NO:281/SEQ ID NO:282; SEQ ID NO:283/SEQ ID NO:284; SEQ ID NO:285/SEQ ID NO:286; SEQ ID NO:287/SEQ ID NO:288; SEQ ID NO:289/SEQ ID NO:290; SEQ ID NO:291/SEQ ID NO:292; SEQ ID NO:293/SEQ ID NO:294; SEQ ID NO:295/SEQ ID NO:296; SEQ ID NO:297/SEQ ID NO:298; SEQ ID NO:299/SEQ ID NO:300; SEQ ID NO:301/SEQ ID NO:302; SEQ ID NO:303/SEQ ID NO:304; SEQ ID NO:305/SEQ ID NO:306; SEQ ID NO:307/SEQ ID NO:308; SEQ ID NO:309/SEQ ID NO:310; SEQ ID NO:311/SEQ ID NO:312; SEQ ID NO:315/SEQ ID NO:316; SEQ ID NO:317/SEQ ID NO:318; SEQ ID NO:319/SEQ ID NO:320; and, SEQ ID NO:321/SEQ ID NO:322.

Although preferred, this disclosure is not limited to each pair as indicated, per se. The population of VL and VH region species disclosed herein can be employed to form distinct pairs i.e., diverse Fabs selected from the population of VL and VH species regions provided.

Example antibodies otherwise functionally described herein are provided wherein the anti-CD47 VL is selected from the group consisting of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:5, SEQ ID NO:7, SEQ ID NO:9, SEQ ID NO:11, SEQ ID NO:13, SEQ ID NO:15, SEQ ID NO:17, SEQ ID NO:19, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:29, SEQ ID NO:31, SEQ ID NO:33, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:53, SEQ ID NO:55, SEQ ID NO:57, SEQ ID NO:59, SEQ ID NO:61, SEQ ID NO:63, SEQ ID NO:65, SEQ ID NO:67, SEQ ID NO:69, SEQ ID NO:71, SEQ ID NO:73, SEQ ID NO:75, SEQ ID NO:77, SEQ ID NO:79, SEQ ID NO:81, SEQ ID NO:83, SEQ ID NO:85, SEQ ID NO:87, SEQ ID NO:89, SEQ ID NO:91, SEQ ID NO:93, SEQ ID NO:95, SEQ ID NO:97, SEQ ID NO:99, SEQ ID NO:101, SEQ ID NO:103, SEQ ID NO:105, SEQ ID NO:107, SEQ ID NO:109, SEQ ID NO:111, SEQ ID NO:113, SEQ ID NO:115, SEQ ID NO:117, SEQ ID NO:119, SEQ ID NO:121, SEQ ID NO:123, SEQ ID NO:125, SEQ ID NO:127, SEQ ID NO:129, SEQ ID NO:131, SEQ ID NO:133, SEQ ID NO:135, SEQ ID NO:137, SEQ ID NO:139, SEQ ID NO:141, SEQ ID NO:143, SEQ ID NO:145, SEQ ID NO:147, SEQ ID NO:149, SEQ ID NO:151, SEQ ID NO:153, SEQ ID NO:155, SEQ ID NO:157, SEQ ID NO:159, SEQ ID NO:161, SEQ ID NO:163, SEQ ID NO:165, SEQ ID NO:167, SEQ ID NO:169, SEQ ID NO:171, SEQ ID NO:173, SEQ ID NO:175, SEQ ID NO:177, SEQ ID NO:179, SEQ ID NO:181, SEQ ID NO:183, SEQ ID NO:185, SEQ ID NO:187, SEQ ID NO:189, SEQ ID NO:191, SEQ ID NO:193, SEQ ID NO:195, SEQ ID NO:197, SEQ ID NO:199, SEQ ID NO:201, SEQ ID NO:203, SEQ ID NO:205, SEQ ID NO:207, SEQ ID NO:209, SEQ ID NO:211, SEQ ID NO:213, SEQ ID NO:215, SEQ ID NO:217, SEQ ID NO:219, SEQ ID NO:221, SEQ ID NO:223, SEQ ID NO:225, SEQ ID NO:227, SEQ ID NO:229, SEQ ID NO:231, SEQ ID NO:233, SEQ ID NO:235, SEQ ID NO:237, SEQ ID NO:239, SEQ ID NO:241, SEQ ID NO:243, SEQ ID NO:245, SEQ ID NO:247, SEQ ID NO:249, SEQ ID NO:251, SEQ ID NO:253, SEQ ID NO:255, SEQ ID NO:257, SEQ ID NO:259, SEQ ID NO:261, SEQ ID NO:263, SEQ ID NO:265, SEQ ID NO:267, SEQ ID NO:269, SEQ ID NO:271, SEQ ID NO:273, SEQ ID NO:275, SEQ ID NO:277, SEQ ID NO:279, SEQ ID NO:281, SEQ ID NO:283, SEQ ID NO:285, SEQ ID NO:287, SEQ ID NO:289, SEQ ID NO:291, SEQ ID NO:293, SEQ ID NO:295, SEQ ID NO:297, SEQ ID NO:299, SEQ ID NO:301, SEQ ID NO:303, SEQ ID NO:305, SEQ ID NO:307, SEQ ID NO:309, SEQ ID NO:311, SEQ ID NO:313, SEQ ID NO:315, SEQ ID NO:317, SEQ ID NO:319, and SEQ ID NO:321; and, the anti-CD47 VH is selected from the group consisting of SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:12, SEQ ID NO:14, SEQ ID NO:16, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32, SEQ ID NO:34, SEQ ID NO:36, SEQ ID NO:38, SEQ ID NO:40, SEQ ID NO:42, SEQ ID NO:44, SEQ ID NO:46, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68, SEQ ID NO:70, SEQ ID NO:72, SEQ ID NO:74, SEQ ID NO:76, SEQ ID NO:78, SEQ ID NO:80, SEQ ID NO:82, SEQ ID NO:84, SEQ ID NO:86, SEQ ID NO:88, SEQ ID NO:90, SEQ ID NO:92, SEQ ID NO:94, SEQ ID NO:96, SEQ ID NO:98, SEQ ID NO:100, SEQ ID NO:102, SEQ ID NO:104, SEQ ID NO:106, SEQ ID NO:108, SEQ ID NO:110, SEQ ID NO:112, SEQ ID NO:114, SEQ ID NO:116, SEQ ID NO:118, SEQ ID NO:120, SEQ ID NO:122, SEQ ID NO:124, SEQ ID NO:126, SEQ ID NO:128, SEQ ID NO:130, SEQ ID NO:132, SEQ ID NO:134, SEQ ID NO:136, SEQ ID NO:138, SEQ ID NO:140, SEQ ID NO:142, SEQ ID NO:144, SEQ ID NO:146, SEQ ID NO:148, SEQ ID NO:150, SEQ ID NO:152, SEQ ID NO:154, SEQ ID NO:156, SEQ ID NO:158, SEQ ID NO:160, SEQ ID NO:162, SEQ ID NO:164, SEQ ID NO:166, SEQ ID NO:168, SEQ ID NO:170, SEQ ID NO:172, SEQ ID NO:174, SEQ ID NO:176, SEQ ID NO:178, SEQ ID NO:180, SEQ ID NO:182, SEQ ID NO:184, SEQ ID NO:186, SEQ ID NO:188, SEQ ID NO:190, SEQ ID NO:192, SEQ ID NO:194, SEQ ID NO:196, SEQ ID NO:198, SEQ ID NO:200, SEQ ID NO:202, SEQ ID NO:204, SEQ ID NO:206, SEQ ID NO:208, SEQ ID NO:210, SEQ ID NO:212, SEQ ID NO:214, SEQ ID NO:216, SEQ ID NO:218, SEQ ID NO:220, SEQ ID NO:222, SEQ ID NO:224, SEQ ID NO:226, SEQ ID NO:228, SEQ ID NO:230, SEQ ID NO:232, SEQ ID NO:234, SEQ ID NO:236, SEQ ID NO:238, SEQ ID NO:240, SEQ ID NO:242, SEQ ID NO:244, SEQ ID NO:246, SEQ ID NO:248, SEQ ID NO:250, SEQ ID NO:252, SEQ ID NO:254, SEQ ID NO:255, SEQ ID NO:258, SEQ ID NO:260, SEQ ID NO:262, SEQ ID NO:264, SEQ ID NO:266, SEQ ID NO:268, SEQ ID NO:270, SEQ ID NO:272, SEQ ID NO:274, SEQ ID NO:276, SEQ ID NO:278, SEQ ID NO:280, SEQ ID NO:282, SEQ ID NO:284, SEQ ID NO:286, SEQ ID NO:288, SEQ ID NO:290, SEQ ID NO:292, SEQ ID NO:294, SEQ ID NO:296, SEQ ID NO:298, SEQ ID NO:300, SEQ ID NO:302, SEQ ID NO:304, SEQ ID NO:306, SEQ ID NO:308, SEQ ID NO:310, SEQ ID NO:312, SEQ ID NO:314, SEQ ID NO:316, SEQ ID NO:318, SEQ ID NO:320, and SEQ ID NO:322.

Properties of CD47×CD20 Bispecific Entities of the Present Invention

In vitro affinity measurements with the extracellular domain of the effector antigen, CD47, initially revealed a 100-200-fold decrease in affinity for these variants. In vitro affinity measurements with the extra-cellular domain of CD47 revealed that the variants had a 100-500-fold decrease in affinity. In vivo and in vitro cell based studies with these detuned IgG1 1+1 heterodimer format bispecifics confirmed effector-based cell killing and decreased binding to non-target cell types relative to a monospecific antibody. Anti-CD20 VL: SEQ ID NO:323; anti-CD20 VH: SEQ ID NO:324. Anti-CD20 LC constant region is SEQ ID NO:343. Anti-CD20 HC constant region is SEQ ID NO:345.

Bispecific entities described, exemplified, and claimed herein demonstrate selective binding to CD20-expressing cells, for example, wherein the interaction of CD47 with the macrophage checkpoint inhibitor, signal-regulatory protein alpha (SIRPα), is blocked. This increased selectivity over monospecific anti-CD47 approaches allows for the use of an IgG1 Fc, which engages activating fragment crystallizable gamma receptors (FcγRs) to fully potentiate macrophages to engulf and destroy CD20 positive cells. In comparison to the anti-CD20 antibody rituximab, for example, anti-CD47/anti-CD20 bispecific antibodies described and exemplified herein are more potent in inducing phagocytosis and ADCC in vitro.

In vitro cell-based studies demonstrate that detuned CD47 bispecific entities described herein activate antibody-dependent cellular phagocytosis, complement-dependent cytotoxicity (CDC), and antibody-dependent cellular cytotoxicity (ADCC). See FIGS. 4A-4C and FIGS. 5A-5C. Further, cynomolgus (cyno) monkey pharmacokinetic (PK) and exploratory toxicity (E-tox) studies experiments demonstrate the detuned CD47 bispecifics effectively deplete B-cells and have reduced binding to cynomolgus red blood cells (RBCS) relative to the parental monospecific anti-CD47 antibody, thereby substantially confirming the success and medical value of the target-cell selective strategy described and claimed herein. Species exemplified herein demonstrate favorable pharmacokinetics and depletion of CD20⁺ B cells with minimum deleterious effects seen on hematologic parameters following multiple administrations to nonhuman primates.

In specific embodiments, CD47×CD20 bispecifics provided herein, designated TPP-1360, TPP-1361, TPP-1367, and TPP-1362, comprise heavy and light chain sequences as follows: TPP-1360 comprises (CD47 LC SEQ ID NO:335; HC SEQ ID NO:336)×(CD20 LC SEQ ID NO:331; HC SEQ ID NO:332). TPP-1361 comprises (CD47 LC SEQ ID NO:333; HC SEQ ID NO:334)×(CD20 LC SEQ ID NO:331; HC SEQ ID NO:332). TPP-1367 comprises (CD47 LC SEQ ID NO:337; HC SEQ ID NO:338)×(CD20 LC SEQ ID NO:331; HC SEQ ID NO:332). TPP-1362 comprises (CD47 LC SEQ ID NO:385; HC SEQ ID NO:386)×(CD20 LC SEQ ID NO:331; HC SEQ ID NO:332).

With regard to TPP-1362, the CD47 VL comprises SEQ ID NO:383. TPP-1362 CD47 VH comprises SEQ ID NO:384. TPP-1362 CD47 VL CDRs comprise SEQ ID NO:377 (CDRL1); SEQ ID NO:378 (CDRL2); and, SEQ ID NO:379 (CDRL3). TPP-1362 CD47 VH CDRs comprise SEQ ID NO:380 (CDRH1); SEQ ID NO:381 (CDRH2); and, SEQ ID NO:382 (CDRH3).

An example series of bispecific entities within the genera otherwise described herein are demonstrated to exhibit pharmacology characteristics generally indicative of the therapeutic value of the genera.

These highly evaluated species, for example, exhibit high affinity to CD20 and detuned affinity to CD47, showing effective CD47 blocking, cyno-cross reactivity, good physicochemical properties (solubility, stability, expression), and low immunogenicity prediction (EpiVax). See Example 13, FIG. 18. The IgG1 heterodimer format and Fc confer reliable production in sufficient amounts and purity using standard CHO processes, with phase appropriate titer, yield, product quality and liquid formulation. These example highly evaluated species exhibit in vitro phagocytosis capacity of CD20⁺ tumor cells superior to CC-90002 and more potent ADCC than rituximab. These example highly evaluated species also exhibit marked reduction in cyno B cells in peripheral blood and lymphoid tissues. These example highly evaluated species also exhibit minimal sink effects with no binding to CD20⁻ CD47⁺ healthy cells (RBC and platelets). These example highly evaluated species also exhibit acceptable PK parameters to support weekly, for example, dosing.

RBC binding capacity of TPP-1360, for example, was extensively evaluated in purified human RBCs and in co-culture of human RBCs with tumor cells. As illustrated in FIG. 8, TPP-1360 is demonstrated to selectively bind CD47⁺/CD20⁺ Raji Cells but Not CD47⁺/CD20⁻ human RBCs. Moreover, in a co-culture of Raji cells and human RBCs, TPP-1360 displayed dose-dependent binding to CD47⁺/CD20⁺ Raji cells but no binding to human RBCs, even at concentration as high as 1 mg/mL. See, FIG. 9. To the contrary, the CD47 wild type/CD20 bispecific, TPP-2, significantly bound to both Raji cells and human RBCs. In addition, TPP-1360 does not show binding to purified cyno RBC from multiple donors.

TPP-1360, an example species bispecific entity of the present disclosure, is a first-in-class antibody, co-targeting CD47 and CD20, designed to bind CD20 with high affinity and CD47 with optimally detuned affinity. When bound to CD20 expressing cells, TPP-1360, for example, not only blocks macrophage checkpoint inhibitor SIRPα interaction with CD47 but also engages activating FcγRs to fully potentiate macrophages to engulf and destroy CD20 positive cells. Potent in vitro activity is induced by TPP-1360, for example, to eliminate cancer cells via multiple modes of action, including phagocytosis, ADCC and CDC. TPP-1360, exemplary of the bispecific entities described herein, provides enhanced pharmacological activities over rituximab and CC-90002.

CD47×CD20 bispecific entities described and claimed herein demonstrate enhanced phagocytosis compared to rituximab or CC-90002 as a single agent. Phagocytosis activity of CD47×CD20 bispecific entities described herein generally correlate with their CD47 binding affinity. CD47×CD20 bispecific entities described herein single agent activity is equivalent to the combination of CC-90002 and rituximab in inducing phagocytosis.

CD47×CD20 bispecific entities described herein demonstrate improved ADCC in rituximab sensitive and resistant tumor cells as compared to single agent anti-CD47 activity.

CD47×CD20 bispecific entities described herein demonstrate better efficacy than rituximab in vivo in Raji NOD-SCID model. See Example 15.

TPP-1360 enhances both phagocytosis and ADCC activity over rituximab. In addition, TPP-1360 and related bispecific entities described, exemplified, and claimed herein, differentiate from CD20×CD3 bispecific T-cell engagers such as REGN1979 from Regeneron, or mosunetuzumab from Roche, now in the clinic as it has different modes of action, including phagocytosis, ADCC and CDC, compared to T cell activation. Furthermore, the toxicity profile is different from CD20×CD3 (potential hematologic toxicity vs cytokine release syndrome). Particularly, T-cell engagers are potent immune engagers that have the potential to trigger apoptosis of non-target cells which express very low levels of the target antigen, therefore either the target antigen needs to be extremely specific or the anti-targeting arm of the bispecific needs to employ either a masking technology or be tuned to differentiate between the levels of expression of the target antigen on normal and disease tissue. Additionally, the anti-CD3 portion of the bispecific needs to be precisely tuned to prevent cytokine release due to systemic activation of T-cells. Importantly, TPP-1360, as a representative example herein, demonstrates favorable elimination kinetics with minimum deleterious effects seen on hematologic parameters following multiple administrations to nonhuman primates. CD47×CD20 bispecific antibodies of the present invention are developed inter alio as intravenous (IV) injectable treatment for B-lymphoma patients, for example, refractory and/or resistant to current therapies.

Bispecific entities described herein are provided for methods of treatment and/or control of tumors, tumor cells, cancer, including but not limited to cells undergoing aberrant proliferation, hematological oncology conditions, hematological malignancies, lymphoproliferative disorders, B-cell disorders, B-cell malignancies, and/or B-cell lymphoma. Bispecific entities of the present invention are formulated and administered according to and consistent with the current state of the art of antibodies as therapeutic entities. Standards of formulation and administration of IgG1 antibodies, for example, are well-known in the art. Antibodies described herein are administered, for example, as an intravenous (IV) injectable treatment for CD20 positive B cell lymphoma patients. The invention is directed to a method of controlling tumor cells comprising administering an effective amount of a bispecific entity described herein to a patient in need thereof. Tumor cells refer to cancer cells including but not limited to cells undergoing aberrant proliferation, hematological oncology conditions, hematological malignancies, lymphoproliferative disorders, B-cell disorders, B-cell malignancies, and B-cell lymphoma.

CD47×CD20 bispecific entities described herein are particularly provided to be employed in a method treatment of a B-cell disorder or a B-cell malignancy comprising administering an effective amount of a bispecific entity described herein to a patient in need thereof.

Allometry and Human Pharmacokinetics are evaluated for bispecific entities described herein. The entities of the present invention comprise a detuned CD47 binding arm and a regular CD20 (rituximab) binding arm. Given the detuned binding affinity of the CD47 arm, the target-mediated drug disposition (TMDD) for the bispecific entities is potentially primarily driven by the CD20 binding. Accordingly, in certain embodiments, the clinical doses will be in the ranges of what is currently used for rituximab. Based on the 10, 20 and 100 mg/kg doses in cynomolgus monkeys, the terminal half-life is approximately 7 days. CD20 mediated TMDD is based on additional preclinical and clinical data for rituximab. The first-in-human clinical study is an open-label, multicenter, Phase 1/1b study to evaluate the safety and tolerability in subjects with relapsed or refractory CD20+ NHL who have progressed on rituximab and/or other CD20-targeted therapies. Dose escalation begins at less than 1 mg/kg and then escalates to 10 mg/kg, which is the current clinical dose for rituximab. Cynomolgus monkeys were dosed twice at 20 mg/kg, on day 1 and day 15. Bispecific entities described herein are found to be well tolerated as single agent in NHP eTOX study with dose-proportional exposure. Mammalian or human dosage of bispecific entities described herein is within the range of about 3 mg/kg to about 20 mg/kg. Further mammalian or human dosage of bispecific entities described herein is particularly within the range of about 5 mg/kg to about 15 mg/kg. Mammalian or human dosage of bispecific entities described herein is also between about 7 mg/kg and about 13 mg/kg. Dosage regimen of bispecific entities described herein is about once every five (5) days, or about once a week (seven (7) days), or about once every ten (10) days, or about once every two (2) weeks.

A manufacturing process for bispecific antibodies described herein may follow a typical Chinese Hamster Ovary (CHO) manufacturing platform. A common contaminant observed in the purification of these bispecific antibodies is the half-antibody, which requires specific purification protocols to remove. After expression of the 4 chain bispecific in Chinese Hamster Ovary cell, protein A is used as the first step to purify an IgG based bispecific. Following this first step there are generally two species present, the desired 4 chain bispecific and a half-antibody. In most cases ion exchange chromatography is sufficient to separate these two species, but in others hydrophobic interaction chromatography may be required. Correct pairing of the LCs should be assessed by mass spectrometry and mis-assembled impurities should be removed by additional protein purification methods, such as ion exchange or hydrophobic interaction chromatography. Following either secondary purification approach, preparative size exclusion chromatography (SEC) can be used to polish and ensure conformational homogeneity, while buffer exchanging the 4 chain bispecifics. Final quality control should include analytical SEC, mass spectrometry, and in vito binding assessments with the different antigens to ensure the conformational and chemical integrity of the bispecific. See, e.g., J. B. Ridgway et al., Protein Eng. 9 (1996) 617-621. K. Gunasekaran et al., J. Biol. Chem. 285 (2010) 19637-19646. Preferred monomeric elements of the IgG1 1+1 heterodimers described herein each contain certain LC and HC constant region sequences discussed supra and identified herein to reduce propensity for homodimer formation during production of the IgG1 1+1 heterodimer format.

EXAMPLES Example 1: Detuning of CC-90002

Rational design to decrease the affinity of the non-detuned parental version of CC-90002 (408_437) anti-CD47 arm was enabled with a crystal structure of an anti-CD47 Fab bound to the extra cellular domain of CD47. The epitope bound by CC-90002 is identical to that of original murine anti-CD47 2A1 bound to human CD47. See, U.S. Pat. No. 9,045,541.

The variable domains of 2A1 were humanized and the final antibody was named “ON” composed of HC_2.3Q and LC_N, which ultimately was developed as an IgG4 PIE format (CC-90002). QN was further modified by the introduction of residues into the variable heavy domain for improved cell-free expression, this HC variant was named “HC_Q_5_MUT”. The HC_Q_5_MUT HC and LC_N were further modified to decrease their immunogenicity using in silico modeling and in silico prediction of immunogenicity, these were collectively referred to as “CD47 2.0”. Further variants in the variable heavy and variable light domains of CD47 2.0 LC_1147_2 and CD47 2.0 HC_434 were designed for improved pharmacokinetics, these were referred to as “CD47 3.0”. WO2016109415 (US.20170369572); WO2018009499 (US.20190241654); and WO2018183182, each of which are herein incorporated by reference.

The anti-CD47 epitope covers a large surface area and residues from both the light chain (LC) and the heavy chain (HC) participate in the interaction.

To decrease the affinity of the anti-CD47 arm for CD47, CD47 interacting residues from both the LC and HC were subjected to in silico mutagenesis using the “Residue Scan” module from the Molecular Operating Environment (MOE) modeling program. This process created a library of thousands of variants with a wide range of predicted affinities. Each in silico Fab variant was modeled to calculate a predicted change in stability (dStability) or a change in affinity for the CD47 ECD (dAffinity). Over 5,000 variants with positive dAffinity scores (predicted to have lower affinity relative to the parental Fab) and negative dStability (predicted to have higher stability than the parental Fab) were analyzed using immunogenicity assessment software to identify variants that would be predicted to have low immunogenicity. Of these, 143 low immunogenic risk Fab variants with predicted Kds for CD47 ranging from 10 nM to 1 mM, were selected for cell based testing.

To screen target-cell selective anti-CD47 Fabs, the selected anti-CD47 Fab variants were constructed as IgG1 fusions and paired with the anti-EGFR arm from cetuximab. The proper assembly of the 4 chain bispecific was enabled by the presence of Fab and Fc substitutions described herein present in all 4 chains. The 4 chain bispecifics containing the 143 selected variants were transiently expressed in Expi-CHO cells and the bispecifics were purified in a single step using magnetic protein A beads. To identify the target-cell selective bispecifics, the variants were tested with two experiments. The first experiment measured the ability of the detuned anti-CD47×anti-EGFR bispecifics to bind to the non-target Raji cell line that expressed the CD47 antigen, but not the EGFR antigen. The second experiment measured the ability of the detuned anti-CD47× anti-EGFR bispecifics to block SIRPα binding to the target Fadu cell line that expressed the CD47 antigen and the EGFR antigen. These experiments, yielded a set of 8 variants that showed a 10-fold to 20-fold decreased affinity for the non-target CD47+/EGFR-Raji cell line relative to the non-detuned anti-CD47× anti-EGFR parental antibody, and yet was still able to block 75-90% SIRPα binding to the CD47+/EGFR+ Fadu target cell line.

The rituximab anti-CD20 arm was paired with the 8 detuned anti-CD47 variants similarly using an IgG1 Fc. It was observed that the detuned CD47×CD20 bispecifics had reduced binding to the CD47+/CD20− non-target Fadu cell line relative to the non-detuned CD47×CD20 parental antibody, and yet were still able to block 75-90% of SIRPα binding to the target Raji cell line which was CD47 and CD20 positive.

Additional developability assessments of the variants led to the selection of a single anti-CD47 Fab variant, VH E59Y/S102E, which was cloned into three CC-90002 derived frameworks, for pharmacokinetic testing in cynomolgus monkeys: TPP-1367, TPP-1360, and TPP-1361.

Example 2: Summary of SPR Binding Results for Bispecific Entities Described Herein

Surface Plasmon Resonance (SPR) experiments were used to measure the affinities of TPP-1360 and TPP-1362 to CD47. These two antibodies were tested for binding to human CD47 and cynomolgus CD47, and were found to not bind to mouse CD47. TPP-1360 was measured to have an affinity for human CD47 ECD of 1.7 μM Kd, which reflects ˜350× decrease in affinity relative to the parental anti-CD47 binder. The TPP-1360 affinity for the cynomolgus CD47 ECD was found to be 4.51 μM Kd. TPP-1362 was measured to have an affinity for human CD47 ECD of 0.796 μM Kd, which reflects ˜150× decrease in affinity relative to the parental anti-CD47 binder. The TPP-1362 affinity for the cynomolgus CD47 ECD was found to be 2.06 μM Kd. Finally, in addition to the measured affinities, a sandwich SPR assay demonstrated that both bound CD47 and CD20 simultaneously.

Example 3: Dose Response of Binding and SIRPα Blocking of Example Bispecific Entities

Dose response curves for TPP-1360 and TPP-1362 blocking of human SIRP∝ binding to various CD20 expressing non-Hodgkins lymphoma tumor cell lines were generated. Cell lines were incubated with increasing concentrations of either bispecific, then human SIRPα was added at a saturating concentration. In addition to the bispecific, rituximab and the parental anti-CD47 binder (TPP-23 which is 408_437 with IgG1) were included for reference. Cells were washed then incubated with a secondary antibody to measure the amount of SIRPα bound to the tumor cells. For cell line OCI-Ly3 (a DLBCL cell line), TPP-1360 was found to have an EC50=1.30 nM and TPP-1362 was found to have an EC50=0.70 nM. For the Raji cell line (a B-lymphocyte Burkitt's lymphoma cell line) TPP-1360 was found to have an EC50=1.64 nM and TPP-1362 was found to have an EC50=1.10 nM. The parental anti-CD47, TPP-23, was found to have an IC₅₀ of 0.11 nM for blocking human SIRPα binding to OCI-Ly3 cells as shown in FIG. 21. Rituximab had no effect on SIRPα binding.

Example 4: Dose Response for Phagocytosis

Dose response curves for TPP-1360 and TPP-1362 activation of phagocytosis towards various CD20 expressing non-Hodgkins lymphoma tumor cell lines were generated. Human monocytes were differentiated into macrophages, which were then added to tumor cell lines that had been incubated with increasing concentrations of either bispecific. In addition to the bispecific entities, rituximab and the parental anti-CD47 binder (TPP-23) were included for reference. Fluorescence labeling of macrophages and tumor cells was used to measure the number of phagocytic events using an image based quantification method. For the OCI-Ly3 cell line, TPP-1360 was found to have an IC50=1.4 nM and TPP-1362 was found to have an IC50=0.43 nM. For the Raji cell line, TPP-1360 was found to have an IC50=1.8 nM and TPP-1362 was found to have an IC50=0.37 nM.

Example 5: Binding Studies with Human and Cyno RBCs and Hemagluttination

Binding of certain bispecific entity examples to human and cynomolgus monkey RBCs was determined to assess their non-target cell binding potential. RBCs were isolated from whole blood and were incubated with increasing concentrations of the example bispecifics. Binding was expressed as a percentage of the amount of binding observed at 2 μg/ml of the parental anti-CD47 binder (TPP-23). At 200 μg/ml, TPP-1360 and TPP-1361 bound to <1% of that seen for the parental anti-CD47 binding to human RBCs. Similarly, at 200 μg/ml, TPP-1360 bound to <1% of that seen for the parental anti-CD47 binding to cynomolgus RBCs. A higher degree of binding was observed for TPP-1362 binding to cynomolgus RBCs at 200 μg/ml, which showed a binding of 2-3% of the parental anti-CD47 binder. Finally, the parental anti-CD47 binders for both leads demonstrated no hemagluttination of human RBCs at 200 μg/ml. Similarly, both TPP-1360 and TPP-1361 showed no hemagluttination at 200 μg/ml. BRIC6, a known hemagluttinating antibody was used as a positive control.

Example 6: Binding Studies to Human PBMCs and Whole Blood

Binding of the bispecific entity species described herein to human Peripheral Blood Mononuclear Cells (PBMCs) was assessed. Relative to the parental anti-CD47 binder TPP-23 and rituximab, the TPP-1360 bispecific showed less binding to all cell types with the exception of the B-cells, which showed significant binding through the presence of the anti-CD20 Fab portion.

Example 7: First Round Lead Cynomolgus PK

A cynomolgus PK experiment was carried out with example bispecific entity species described herein. Cynomolgus monkeys were dosed twice at 20 mg/kg, on day 1 and day 15. B-cell depletion was observed. From these studies TPP-1360 and TPP-1362 were chosen for further study in a cynomolgus monkey exploratory toxicology (E-tox) study, as described in Example 8.

Example 8: Second Round Lead Cynomolgus E-Tox

A cynomolgus E-tox experiment was carried out with TPP-1360, and TPP-1362. For TPP-1360, cynomolgus monkeys were dosed at 100, 20, and 10 mg/kg, once a week for two weeks, which was followed by a non-dosing period of 2 weeks. A second TPP-1360 arm, tested 10 mg/kg twice a week for two weeks, which was also followed by a two week non-dosing period. For TPP-1362, cynomolgus monkeys were dosed at 60, 20, and 10 mg/kg, once a week for two weeks, which was followed by a non-dosing period of 2 weeks. A second TPP-1362 arm, tested 10 mg/kg twice a week for two weeks, which was also followed by a two week non-dosing period, twice at 20 mg/kg, on day 1 and day 15. These studies showed that TPP-1360 was well tolerated, showed deep B-cell depletion, and achieved dose-proportional exposure, confirming the avoidance of sink thus the target-cell selective.

Example 9: In Vitro Pharmacology A. Human Whole Blood Binding

To assess the specificity of TPP-1360, its binding profile was first evaluated in whole blood using flow cytometry. Across two donors, 200 nM TPP-1360 substantially shifted the binding signal to B cells and rather weakly to T cells, monocytes, and NK cells, with minimal or no binding to platelets or red blood cells thereby illustrating selective binding to B cells in human whole blood. See, FIG. 7.

FIG. 7 shows that the bispecific TPP-1360, for example, binds primarily to B cells, with a very small amount of binding to the other cell types listed possibly because of higher levels of CD47 than what is found on blood cells, or because of the contribution of the Fc which can engage Fc receptors which are expressed on NK cells and monocytes. Conversely TPP-23, a high affinity CD47 monospecific antibody binds to all of these cell types due to the ubiquitous expression of CD47 and the high affinity for CD47 found in TPP-23.

The overall binding profile of TPP-1360 in human whole blood is similar to rituximab. Conversely, the parental CD47 mAb, TPP-23, used as a control for CD47 expression, significantly bound to all cell populations in human blood.

B. Tumor Cell Binding

Furthermore, the RBC binding capacity of TPP-1360, for example, was extensively evaluated in purified human RBCs and in co-culture of human RBCs with tumor cells. As illustrated in FIG. 8, TPP-1360 selectively bound CD47⁺/CD20⁺ Raji Cells but not CD47⁺/CD20⁻ human RBCs. Moreover, in a co-culture of Raji cells and human RBCs, TPP-1360 displayed dose-dependent binding to CD47⁺/CD20⁺ Raji cells but no binding to human RBCs, even at concentration as high as 1 mg/mL. See, FIG. 9. To the contrary, the parental CD47 type/CD20 bispecific, TPP-2, significantly bound to both Raji cells and human RBCs. In addition, TPP-1360 does not show binding to purified cyno RBC from multiple donors.

C. SIRPα Competition

Having demonstrated its selective binding to CD20⁺/CD47⁺ cells, an assessment was made of the ability of TPP-1360 to antagonize human SIRPα interaction with cell surface CD47 using an in vitro competition assay. TPP-1360 potently and blocked recombinant human SIRPα-Fc binding to human CD47 expressed on the surface of CD20⁺/CD47⁺ lymphoma cell lines OCI-Ly3 and Raji, with average EC50 values of 1.30 nM and 1.64 nM, respectively. See, FIG. 10 and FIG. 11. FIG. 10 illustrates the fact that TPP-1360, for example, potently and completely blocked recombinant human SIRPα-Fc binding to human CD47 expressed on the surface of CD20⁺/CD47⁺ lymphoma cell line OCI-Ly3. FIG. 11 illustrates the fact that TPP-1360, for example, potently and completely blocked recombinant human SIRPα-Fc binding to human CD47 expressed on the surface of CD20⁺/CD47⁺ lymphoma cell line Raji. In contrast, neither rituximab nor control bispecific antibody TPP-1480 (anti-CD20/hen egg lysozyme) were able to compete with human SIRPα-Fc binding to the same cell lines. The data presented herein also demonstrates that TPP-1360 potency to block human SIRPα-CD47 interaction is lower than TPP-23, consistent with the attenuated affinity of TPP-1360 to human CD47.

Example 10: Functional Activities: Human Macrophage Phagocytosis

This Example demonstrates the capacity of TPP-1360 in triggering tumor phagocytosis, as determined in vitro by automated counting of “eaten” CD20⁺ CD47⁺ tumor cells inside of labeled macrophages.

Expression of CD20 and CD47 was first verified in each target tumor cell line (OCI-Ly3, Raji, REC-1, and RIVA) by quantifying antibody binding capacity (ABC) using a flow cytometric assay (Denny T N et al., Cytometry. 1996 December; 26(4):265-74). All four cell lines express high levels of CD47 and CD20. Table 1.

TABLE 1 CD47 and CD20 Antigen Expression on Lymphoma Cell Surface Cell Line CD20 ABC CD47 ABC OCI-Ly3 154,000 247,000 REC-1 510,036 453,415 RIVA 722,000 443,000 Raji 522,596 213,927 ABC = Antibody binding capacity.

Next, titrated antibodies were added to pre-differentiated macrophages, followed by co-culture with carboxyfluorescein succinimidyl ester (CSFE)-labeled tumor cells opsonized with TPP-1360. Phagocytosis activity was quantitatively determined by the number of labeled tumor cells within the labeled macrophages. Green intensity (CFSE) was measured in each of the CD14 allophycocyanin (APC)-labeled macrophages, and a threshold gate was used to identify CFSE-positive macrophages. A threshold of approximately 1000 MFI (mean fluorescence intensity), with a variance of no more than a few hundred MFI was observed across the experiments. For each sample, the calculated percentage of phagocytosis was determined as: [(Number of CFSE-positive macrophages)/(number of total macrophage)]×100. Across at least two donors, treatment with TPP-1360 induced macrophage-mediated phagocytosis of four CD20⁺ malignant B cell lines. Representative data from one donor is shown in FIG. 12 (Raji cells), FIG. 13 (OCI-Ly3 cells), FIG. 14 (REC-1 cells), and FIG. 15 (RIVA cells). Area under the curve was calculated and followed by paired t test to determine statistical significance of TPP-1360 compared with rituximab. See, FIG. 16. The data demonstrates that treatment with TPP-1360 triggered significantly more efficient phagocytosis than rituximab in Raji and OCI-Ly3 cells, likely due to the concomitant blockade of the SIRPα-CD47 interaction and the engagement of activating receptors, such as FcγRs, by TPP-1360.

Example 11: Pharmacokinetics

To determine the pharmacokinetic (PK) profile of the bispecific entities (antibody species, TPP-1360, TPP-1361, TPP-1362 and TPP-1367 described herein, non-GLP studies were conducted in mice and cynomolgus monkeys. A single-dose mouse PK study was performed using naïve, female, NOD/SCID mice with 10 mg/kg of antibody administered via intraperitoneal (IP) injection. Sparse PK sampling (n=4 per timepoint) was performed over the course of 72 hours, and all animals showed detectable antibody species concentrations throughout study duration. The calculated half-life was 3.4 days but may be underestimated considering the sampling duration. To evaluate the PK profiles in cynomolgus monkeys, a repeat-dose exploratory toxicology study was performed, and 20 mg/kg of antibody species was administered via IV bolus injection on Day 1 and Day 15 to three naïve male monkeys. Following repeat-dosing of the antibody species, systemic exposure was achieved, and the antibody species was detectable in the serum of 2 of 3 monkeys throughout study duration (336 hr post Day 15 dose). Samples were also collected as part of the repeat-dose study for hematology and immunophenotyping assessments. The observed depletion of B-lymphocytes demonstrates drug functionality in vivo. Overall, antibody species exposure was maintained throughout study duration in both the single-dose mouse and repeat-dose monkey studies with similar half-lives ranging from 3-3.5 days reported between the two studies.

Example 12: Safety Profile

This example series of highly evaluated species exhibit acceptable toxicology profile, e.g., well tolerated up to 100 mg/kg QW, the highest dose tested. Toxicokinetics were evaluated as part of a 28-day exploratory toxicology study in cynomolgus monkeys. TPP-1360 was administered either BIW or QW via IV injection to cynomolgus monkeys (4/group) at dose levels of 10 mg/kg (BIW) on Days 1, 4, 8, 11, and 15 or at 20 and 100 mg/kg (QW) on Days 1, 8, and 15. Serum concentrations were measured with a sandwich ELISA using an anti-rituximab antibody for capture and a goat anti-human IgG Fc for detection. Following multiple IV doses of 10, 20, or 100 mg/kg, systemic exposure of TPP-1360 was achieved at all dose levels and maintained by all animals throughout study duration. TPP-1360 exhibited linear TK with approximately dose proportional increases in C_(max) and AUC₀₋₁₆₈ across the 20 and 100 mg/kg dose groups. After first dose, clearance was similar across the 10-100 mg/kg dose range, suggesting target saturation at 10 mg/kg dose. R_(AUC) values indicate some TPP-1360 accumulation by Dose 5 and Dose 3 in the 10 (BIW) and 100 (QW) mg/kg dose groups, respectively. The mean calculated half-life ranged from 2-4 days depending on the dose level and dose regimen. Anti-drug antibody was detected in 5/8 animals tested at Day 15 prior to dose and in 5/6 animals tested on study Day 29. Anti-drug antibodies did affect the exposure of TPP-1360 as evidenced by an observed decrease in exposure for ADA positive animals. TPP-1360 was well-tolerated up to 100 mg/kg QW, the highest dose tested. Decreases in B cells in the peripheral blood and in multiple lymphoid tissues were seen at 10 mg/kg BIW and 20 mg/kg QW, demonstrating robust pharmacodynamic activity. Dosing 10 mg/kg BIW did not provide added benefit over 20 mg/kg QW. In addition to effects on B cells, TPP-1360 also decreased T cells and NK cells at all dose levels, neutrophils at 20 mg/kg QW and red blood cells at 100 mg/kg QW. However, no test article-related decrease of platelets was observed. Decreases in T cells, NK cells, neutrophils and red blood cells are believed to be mediated by the CD47 arm of TPP-1360, since these cells do not express CD20.

Example 13: Immunogenicity

The Interactive Screening and Protein Reengineering Interface (ISPRI) software, developed by EpiVax, is an in silico computational method used to assess potential antibody immunogenicity in humans, and is known to be a clinically well-established T cell-dependent analysis tool (FIG. 18). The VH and VL amino acid sequences of TPP-1360 were analyzed for putative T effector and T regulatory hotspots and were found to have a low risk for immunogenicity.

Example 14: Raji Xenograft Model

CD47×CD20 bispecific entities described herein demonstrate better efficacy than rituximab in vivo in a Raji NOD-SCID model. The purpose of this study was to determine the single agent antitumor activity of TPP-1360 or TPP-1362 in a Raji xenograft model expressing lower levels of CD20 and higher levels of CD47. Female NOD-SCID mice were inoculated with Raji cells in the right flank. Dosing was initiated when the tumors were approximately 270 mm³ in size. TPP-1360 and TPP-1362 were tested at 10 and 30 mg/kg with a once a week (QW) dosing for 2 weeks. Rituximab which is bivalent to CD20 was used as a comparator with the same dosing paradigm. The final tumor volume reduction was determined on Day 25 at the time of the termination of the study when the mean tumor volumes in the isotype control (anti-RSV IgG1) group reached approximately 2000 mm³. Significant (p<0.0001) antitumor activity of TPP-1360 with a tumor volume reduction of 52% was observed at both 10 and 30 mg/kg, QW, and also significant antitumor activity of TPP-1362 with a tumor reduction of 62% was observed at 10 mg/kg QW or 64% at 30 mg/kg QW. (FIGS. 19-20) In the same dosing regimen, rituximab showed a 33% and 38% TVR at 30 and 10 mg/kg, respectively. The antitumor activity of TPP-1360 at 30 mg/kg, QW was significantly (p<0.01) better than rituximab at corresponding dose level, suggesting the contribution of CD47 arm in the antitumor activity of TPP-1360. The antitumor activity of TPP-1362 at 30 mg/kg, QW was also significantly (p<0.0001) better than rituximab at corresponding dose level, suggesting the contribution of CD47 arm in the antitumor activity of TPP-1362. There was no significant body weight loss in the animals treated with isotype control, TPP-1360, TPP-1362 or rituximab.

Sequence Listing SEQ ID NO: Description Amino Acid Sequence 1 CG_64_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYAEFPYTFGGGTKVEIK 2 CG_64_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGYI DPEQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 3 CG_65_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYQEFPYTFGGGTKVEIK 4 CG_65_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGYI DPTQGDTHYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 5 CG_66_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYEEFPYTFGGGTKVEIK 6 CG_66_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGYI DPSQGDTVYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 7 CG_67_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHDYLSWFQQKPGKVPKHLIYRANIL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 8 CG_67_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI YPDQGVTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 9 CG_68_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHDYLSWFQQKPGKVPKHLIYRANLL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 10 CG_68_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI EPDQGATEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 11 CG_69_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHDYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 12 CG_69_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI HPDQGITEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 13 CG_70_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANAL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 14 CG_70_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI LPDQGVTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 15 CG_71_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANILV SGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 16 CG_71_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI EPDQGITEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSYP MDYWGQGTLVTVSS 17 CG_72_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANLL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 18 CG_72_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI LPDQGITEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSYP MDYWGQGTLVTVSS 19 CG_73_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 20 CG_73_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI IPDQGMTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 21 CG_74_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANVL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 22 CG_74_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI MPDQGLTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 23 CG_75_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 24 CG_75_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI MPDQGITEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 25 CG_76_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHIYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 26 CG_76_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI MPDQGMTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 27 CG_77_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHIYLSWFQQKPGKVPKHLIYRANTLV SGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 28 CG_77_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI YPDQGMTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 29 CG_78_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHLYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 30 CG_78_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI QPDQGLTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 31 CG_79_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHLYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 32 CG_79_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI EPDQGYTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 33 CG_80_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHNYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 34 CG_80_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI LPDQGYTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 35 CG_81_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHNYLSWFQQKPGKVPKHLIYRANVL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 36 CG_81_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI FPDQGMTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 37 CG_82_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHQYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 38 CG_82_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI YPDQGITEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSYP MDYWGQGTLVTVSS 39 CG_83_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHQYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 40 CG_83_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI FPDQGQTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 41 CG_84_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHTYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 42 CG_84_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI YPDQGLTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 43 CG_85_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHTYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 44 CG_85_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI HPDQGLTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 45 CG_86_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHVYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 46 CG_86_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI HPDQGVTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 47 CG_87_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHYYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 48 CG_87_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI YPDQGATEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 49 CG_88_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHVYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 50 CG_88_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI YPDQGATEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 51 CG_89_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHTYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 52 CG_89_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI SPDQGSTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 53 CG_90_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 54 CG_90_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI MPDQGYTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 55 CG_91_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHLYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 56 CG_91_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI IPDQGYTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSYP MDYWGQGTLVTVSS 57 CG_92_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHVYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 58 CG_92_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI EPDQGMTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 59 CG_93_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHHYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 60 CG_93_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI APDQGVTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 61 CG_94_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHVYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 62 CG_94_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI VPDQGMTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 63 CG_95_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHTYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 64 CG_95_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI APDQGITEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 65 CG_96_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHIYLSWFQQKPGKVPKHLIYRANELV SGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 66 CG_96_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI MPDQGATEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 67 CG_97_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHYYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 68 CG_97_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI VPDQGITEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 69 CG_98_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHHYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 70 CG_98_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI YPDQGITEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSYP MDYWGQGTLVTVSS 71 CG_99_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHYYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 72 CG_99_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI YPDQGVTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 73 CG_100_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHIYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 74 CG_100_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI EPDQGLTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 75 CG_101_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHYYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 76 CG_101_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI LPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 77 CG_102_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHVYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 78 CG_102_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI YPDQGSTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 79 CG_103_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHIYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 80 CG_103_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGATEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 81 CG_104_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHLYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 82 CG_104_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI QPDQGVTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 83 CG_105_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHLYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 84 CG_105_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI IPDQGETEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSYP MDYWGQGTLVTVSS 85 CG_106_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHDYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 86 CG_106_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI IPDQGTTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSYP MDYWGQGTLVTVSS 87 CG_107_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHTYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 88 CG_107_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI IPDQGYTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSYP MDYWGQGTLVTVSS 89 CG_108_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 90 CG_108_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGDSS YPMDYWGQGTLVTVSS 91 CG_109_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 92 CG_109_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTQYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGYSS YPMDYWGQGTLVTVSS 93 CG_110_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 94 CG_110_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTLYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGESSY PMDYWGQGTLVTVSS 95 CG_111_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 96 CG_111_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTVYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGESS YPMDYWGQGTLVTVSS 97 CG_112_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 98 CG_112_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPQQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGVSS YPMDYWGQGTLVTVSS 99 CG_113_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 100 CG_113_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI LPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGYSSY PMDYWGQGTLVTVSS 101 CG_114_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 102 CG_114_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGATYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 103 CG_115_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 104 CG_115_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDTGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYYSSSY PMDYWGQGTLVTVSS 105 CG_116_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 106 CG_116_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTSYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGYSSY PMDYWGQGTLVTVSS 107 CG_117_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 108 CG_117_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTAYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGLSSY PMDYWGQGTLVTVSS 109 CG_118_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 110 CG_118_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDVGSTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 111 CG_119_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 112 CG_119_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGATSYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 113 CG_120_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 114 CG_120_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI LPDSGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 115 CG_121_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 116 CG_121_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDLGDTSYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 117 CG_122_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 118 CG_122_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGLTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYDSSSY PMDYWGQGTLVTVSS 119 CG_123_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 120 CG_123_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDVGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGVSSY PMDYWGQGTLVTVSS 121 CG_124_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 122 CG_124_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGTTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 123 CG_125_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 124 CG_125_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTLYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGDSS YPMDYWGQGTLVTVSS 125 CG_126_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 126 CG_126_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDLGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 127 CG_127_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 128 CG_127_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKVYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGYSSY PMDYWGQGTLVTVSS 129 CG_128_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 130 CG_128_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGHTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYYSSSY PMDYWGQGTLVTVSS 131 CG_129_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 132 CG_129_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGYSSY PMDYWGQGTLVTVSS 133 CG_130_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 134 CG_130_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPLVGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 135 CG_131_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 136 CG_131_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYVLHWVRQAPGKGLEWMGW IDPDLGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 137 CG_132_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 138 CG_132_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDEGLTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 139 CG_133_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 140 CG_133_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGKSSY PMDYWGQGTLVTVSS 141 CG_134_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 142 CG_134_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI LPDQGDSEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 143 CG_135_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 144 CG_135_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI QPDQGDTAYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 145 CG_136_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 146 CG_136_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI LPDVGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 147 CG_137_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 148 CG_137_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKEYYLHWVRQAPGKGLEWMGWI DPDTGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 149 CG_138_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 150 CG_138_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI LPDGGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 151 CG_139_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 152 CG_139_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGESSY PMDYWGQGTLVTVSS 153 CG_140_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 154 CG_140_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGVSS YPMDYWGQGTLVTVSS 155 CG_141_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 156 CG_141_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYYYSSY PMDYWGQGTLVTVSS 157 CG_142_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDQFPYTFGGGTKVEIK 158 CG_142_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 159 CG_143_VL NIQMTQSPSSLSASVGDRVTITCRASQDIQRYLSWFQQKPGKVPKHLIYYANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 160 CG_143_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 161 CG_144_VL NIQMTQSPSSLSASVGDRVTITCRASQDISRYLSWFQQKPGKVPKHLIYYANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 162 CG_144_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 163 CG_145_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDHFPYTFGGGTKVEIK 164 CG_145_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 165 CG_146_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYYANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYYEFPYTFGGGTKVEIK 166 CG_146_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 167 CG_147_VL NIQMTQSPSSLSASVGDRVTITCRASQDIARYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDVFPYTFGGGTKVEIK 168 CG_147_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 169 CG_148_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDLFPYTFGGGTKVEIK 170 CG_148_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 171 CG_149_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYQEFPYTFGGGTKVEIK 172 CG_149_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 173 CG_150_VL NIQMTQSPSSLSASVGDRVTITCRASQDIYYYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 174 CG_150_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 175 CG_151_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYVEFPYTFGGGTKVEIK 176 CG_151_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 177 CG_152_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYYANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYHEFPYTFGGGTKVEIK 178 CG_152_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 179 CG_153_VL NIQMTQSPSSLSASVGDRVTITCRASQDIERYLSWFQQKPGKVPKHLIYYANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 180 CG_153_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 181 CG_154_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDKFPYTFGGGTKVEIK 182 CG_154_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 183 CG_155_VL NIQMTQSPSSLSASVGDRVTITCRASQDIYTYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 184 CG_155_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 185 CG_156_VL NIQMTQSPSSLSASVGDRVTITCRASQDILRYLSWFQQKPGKVPKHLIYYANRLV SGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 186 CG_156_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 187 CG_157_VL NIQMTQSPSSLSASVGDRVTITCRASQDITRYLSWFQQKPGKVPKHLIYYANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 188 CG_157_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 189 CG_158_VL NIQMTQSPSSLSASVGDRVTITCRASQDIDRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDLFPYTFGGGTKVEIK 190 CG_158_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 191 CG_159_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHVYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYYEFPYTFGGGTKVEIK 192 CG_159_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 193 CG_160_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYAEFPYTFGGGTKVEIK 194 CG_160_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 195 CG_161_VL NIQMTQSPSSLSASVGDRVTITCRASQDILTYLSWFQQKPGKVPKHLIYRANRLV SGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 196 CG_161_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 197 CG_162_VL NIQMTQSPSSLSASVGDRVTITCRASQDIARYLSWFQQKPGKVPKHLIYYANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 198 CG_162_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 199 CG_163_VL NIQMTQSPSSLSASVGDRVTITCRASQDIVTYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 200 CG_163_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 201 CG_164_VL NIQMTQSPSSLSASVGDRVTITCRASQDILEYLSWFQQKPGKVPKHLIYRANRLV SGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 202 CG_164_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 203 CG_165_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYYEFPYTFGGGTKVEIK 204 CG_165_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 205 CG_166_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYYANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDVFPYTFGGGTKVEIK 206 CG_166_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 207 CG_167_VL NIQMTQSPSSLSASVGDRVTITCRASQDILVYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 208 CG_167_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 209 CG_168_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYAEFPYTFGGGTKVEIK 210 CG_168_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 211 CG_169_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYQEFPYTFGGGTKVEIK 212 CG_169_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 213 CG_170_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYEEFPYTFGGGTKVEIK 214 CG_170_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 215 CG_171_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHDYLSWFQQKPGKVPKHLIYRANIL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 216 CG_171_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 217 CG_172_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHDYLSWFQQKPGKVPKHLIYRANLL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 218 CG_172_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 219 CG_173_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHDYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 220 CG_173_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 221 CG_174_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANAL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 222 CG_174_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 223 CG_175_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANILV SGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 224 CG_175_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 225 CG_176_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANLL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 226 CG_176_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 227 CG_177_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 228 CG_177_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 229 CG_178_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANVL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 230 CG_178_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 231 CG_179_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHIYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 232 CG_179_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 233 CG_180_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHIYLSWFQQKPGKVPKHLIYRANTLV SGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 234 CG_180_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 235 CG_181_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHLYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 236 CG_181_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 237 CG_182_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHLYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 238 CG_182_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 239 CG_183_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHNYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 240 CG_183_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 241 CG_184_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHNYLSWFQQKPGKVPKHLIYRANVL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 242 CG_184_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 243 CG_185_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHQYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 244 CG_185_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 245 CG_186_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHVYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 246 CG_186_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 247 CG_187_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHTYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 248 CG_187_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 249 CG_188_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHEYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 250 CG_188_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 251 CG_189_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHLYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 252 CG_189_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 253 CG_190_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHVYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 254 CG_190_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 255 CG_191_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHHYLSWFQQKPGKVPKHLIYRANYL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 256 CG_191_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 257 CG_192_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHIYLSWFQQKPGKVPKHLIYRANELV SGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 258 CG_192_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 259 CG_193_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHYYLSWFQQKPGKVPKHLIYRANEL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 260 CG_193_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 261 CG_194_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHHYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 262 CG_194_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 263 CG_195_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHIYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 264 CG_195_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 265 CG_196_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHYYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 266 CG_196_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 267 CG_197_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHVYLSWFQQKPGKVPKHLIYRANDL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 268 CG_197_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 269 CG_198_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHIYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 270 CG_198_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 271 CG_199_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHTYLSWFQQKPGKVPKHLIYRANQL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 272 CG_199_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 273 CG_200_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 274 CG_200_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 275 CG_201_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRESRFV DGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 276 CG_201_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGESSY PMDYWGQGTLVTVSS 277 CG_202_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 278 CG_202_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDQGDTYYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGESS YPMDYWGQGTLVTVSS 279 CG_203_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 280 CG_203_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGESSY PMDYWGQGTLVTVSS 281 CG_204_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 282 CG_204_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDQGDTYYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGDSS YPMDYWGQGTLVTVSS 283 CG_205_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRESRFV DGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 284 CG_205_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGDSS YPMDYWGQGTLVTVSS 285 CG_206_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 286 CG_206_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGYI DPSQGDTVYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 287 CG_207_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHEYLSWFQQDPGTVPQHLIYRESLF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 288 CG_207_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDQGDTEYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 289 CG_208_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 290 CG_208_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDQGDTAYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGLSS YPMDYWGQGTLVTVSS 291 CG_209_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 292 CG_209_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDQGATYYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 293 CG_210_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 294 CG_210_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDVGSTEYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 295 CG_211_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 296 CG_211_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDQGDTEYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 297 CG_212_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRESRFV DGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYEEFPYTFGGGTKVEIK 298 CG_212_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGLTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 299 CG_213_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYEEFPYTFGGGTKVEIK 300 CG_213_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDQGDTEYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 301 CG_214_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRESRFV DGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYAEFPYTFGGGTKVEIK 302 CG_214_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGLTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 303 CG_215_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYAEFPYTFGGGTKVEIK 304 CG_215_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDQGDTEYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGSSS YPMDYWGQGTLVTVSS 305 CG_216_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYAEFPYTFGGGTKVEIK 306 CG_216_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 307 CG_217_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRESRFV DGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 308 CG_217_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDEGLTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 309 CG_218_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 310 CG_218_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDEGLTEYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS 311 CG_219_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 312 CG_219_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDQGDTYYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGDSS YPMDYWGQGTLVTVSS 313 CG_220_VL NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 314 CG_220_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW IDPDQGDTVYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGESS YPMDYWGQGTLVTVSS 315 CG_221_VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRESRFV DGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 316 CG_221_VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGDSS YPMDYWGQGTLVTVSS 317 TPP-1361 NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF CD47 VL VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 318 TPP-1361 QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW CD47 VH IDPDQGDTYYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGESS YPMDYWGQGTLVTVSS 319 TPP-1360 NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRESRFV CD47 VL DGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 320 TPP-1360 QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI CD47 VH DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGESSY PMDYWGQGTLVTVSS 321 TPP-1367 NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL CD47 VL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 322 TPP-1367 QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI CD47 VH DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGESSY PMDYWGQGTLVTVSS 323 CD20 VL QIVLSQSPAILSASPGEKVTMTCRASSSVSYIHWFQQKPGSSPKPWIYATSNLAS GVPVRFSGSGSGTSYSLTISRVEAEDAATYYCQQWTSNPPTFGGGTKLEIK 324 CD20 VH QVQLQQPGAELVKPGASVKMSCKASGYTFTSYNMHWVKQTPGRGLEWIGAI YPGNGDTSYNQKFKGKATLTADKSSSTAYMQLSSLTSEDSAVYYCARSTYYGGD WYFNVWGAGTTVTVSA 325 90002 VL NIQMTQSPSAMSASVGDRVTITCKASQDIHRYLSWFQQKPGKVPKHLIYRANR LVSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 326 90002 VH QMQLVQSGAEVKKTGSSVKVSCKASGFNIKDYYLHWVRQAPGQALEWMGW IDPDQGDTEYAQKFQDRVTITRDRSMSTAYMELSSLRSEDTAMYYCNAAYGSS SYPMDYWGQGTTVTVSS 327 90002 NIQMTQSPSAMSASVGDRVTITCKASQDIHRYLSWFQQKPGKVPKHLIYRANRLV WHOLE LC/ SGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIKRTV IgG1 AAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESV TEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 328 90002 QMQLVQSGAEVKKTGSSVKVSCKASGFNIKDYYLHWVRQAPGQALEWMGW WHOLE HC/ IDPDQGDTEYAQKFQDRVTITRDRSMSTAYMELSSLRSEDTAMYYCNAAYGSS IgG1 SYPMDYWGQGTTVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPV TVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNT KVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVV DVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLN GKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVK GFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVF SCSVMHEALHNHYTQKSLSLSPGK 329 LC-WHOLE QIVLSQSPAILSASPGEKVTMTCRASSSVSYIHWFQQKPGSSPKPWIYATSNLAS RITUXIMAB GVPVRFSGSGSGTSYSLTISRVEAEDAATYYCQQWTSNPPTFGGGTKLEIKRTVA APSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTE QDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 330 HC-WHOLE QVQLQQPGAELVKPGASVKMSCKASGYTFTSYNMHWVKQTPGRGLEWIGAI RITUXIMAB YPGNGDTSYNQKFKGKATLTADKSSSTAYMQLSSLTSEDSAVYYCARSTYYGGD WYFNVWGAGTTVTVSAASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPV TVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNT KVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVV DVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLN GKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVK GFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVF SCSVMHEALHNHYTQKSLSLSPGK 331 CD20 WHOLE QIVLSQSPAILSASPGEKVTMTCRASSSVSYIHWFQQKPGSSPKPWIYATSNLAS LC GVPVRFSGSGSGTSYSLTISRVEAEDAATYYCQQWTSNPPTFGGGTKLEIKRTVA APSVAIFPPSDERLKSGTASVVCVLNNFYPREAKVQWKVDNALQSGNSQESVT EQDSKDSTYSLSSRLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 332 CD20 WHOLE QVQLQQPGAELVKPGASVKMSCKASGYTFTSYNMHWVKQTPGRGLEWIGAI HC YPGNGDTSYNQKFKGKATLTADKSSSTAYMQLSSLTSEDSAVYYCARSTYYGGD WYFNVWGAGTTVTVSAASTKGPSVFPLAPSSKSTSGGTAWLGCEVTDYFPEPV TVSWNSGALTSGVHTFPAVLESSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNT KVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVV DVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLN GKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYVYPPSREEMTKNQVSLTCLVK GFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFALVSKLTVDKSRWQQGNVF SCSVMHEALHNHYTQKSLSLSPGK 333 TPP-1361 NIQMTQSPSSLSASVGDRVTITCQASQDIHRYLSWFQQDPGTVPQHLIYRESRF CD47 WHOLE VDGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIKRTV LC AAPSVFIFPPSDEELKSGTASVVCWLNNFYPREAKVQWKVDNALQSGNSEESV TEQDSKDSTYSLSSTLELSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 334 TPP-1361 QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGQGLEWMGW CD47 WHOLE IDPDQGDTYYAQKFQGRVTITRDRSTSTAYMELASLTAEDTAVYYCNAAYGESS HC YPMDYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVT VSWNSGALTSGVHTFPAVLKSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTK VDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVD VSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGK EYKCKVSNKALPAPIEKTISKAKGQPREPQVYVLPPSREEMTKNQVSLLCLVKGF YPSDIAVEWESNGQPENNYLTWPPVLDSDGSFFLYSKLTVDKSRWQQGNVFS CSVMHEALHNHYTQKSLSLSPGK 335 TPP-1360 NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRESRFV CD47 WHOLE DGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIKRTVA LC APSVFIFPPSDEELKSGTASVVCWLNNFYPREAKVQWKVDNALQSGNSEESVT EQDSKDSTYSLSSTLELSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 336 TPP-1360 QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI CD47 WHOLE DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGESSY HC PMDYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTV SWNSGALTSGVHTFPAVLKSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKV DKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVD VSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEY KCKVSNKALPAPIEKTISKAKGQPREPQVYVLPPSREEMTKNQVSLLCLVKGFY PSDIAVEWESNGQPENNYLTWPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCS VMHEALHNHYTQKSLSLSPGK 337 TPP-1367 NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL CD47 WHOLE VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIKRT LC VAAPSVFIFPPSDEELKSGTASVVCWLNNFYPREAKVQWKVDNALQSGNSEESV TEQDSKDSTYSLSSTLELSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 338 TPP-1367 QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWI CD47 WHOLE DPDQGDTYYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGESSY HC PMDYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTV SWNSGALTSGVHTFPAVLKSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKV DKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV SHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKE YKCKVSNKALPAPIEKTISKAKGQPREPQVYVLPPSREEMTKNQVSLLCLVKGFY PSDIAVEWESNGQPENNYLTWPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCS VMHEALHNHYTQKSLSLSPGK 339 anti-CD47 RTVAAPSVFIFPPSDEELKSGTASVVCWLNNFYPREAKVQWKVDNALQSGNSE IgG1 LC ESVTEQDSKDSTYSLSSTLELSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC Constant Region 340 anti-CD47 ELKSGTASVVCWLNNFYPREAKVQWKVDNALQSGNSEESVTEQDSKDSTYSLS IgG1 LC STLE Constant Region- underlined portion of SEQ ID NO: 339 341 anti-CD47 ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFP IgG1 HC AVLKSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTC Constant PPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVD Region GVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIE KTISKAKGQPREPQVYVLPPSREEMTKNQVSLLCLVKGFYPSDIAVEWESNGQP ENNYLTWPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQK SLSLSPGK 342 anti-CD47 KSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPC IgG1 HC PAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVE Constant VHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTIS Region- KAKGQPREPQVYVLPPSREEMTKNQVSLLCLVKGFYPSDIAVEWESNGQPENN underlined YLTW portion of SEQ ID NO: 341 343 anti-CD20 RTVAAPSVAIFPPSDERLKSGTASVVCVLNNFYPREAKVQWKVDNALQSGNSQ IgG1 LC ESVTEQDSKDSTYSLSSRLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC Constant Region 344 anti-CD20 AIFPPSDERLKSGTASVVCVLNNFYPREAKVQWKVDNALQSGNSQESVTEQDS IgG1 LC KDSTYSLSSR Constant Region- underlined portion of SEQ ID NO: 343 345 anti-CD20 ASTKGPSVFPLAPSSKSTSGGTAWLGCEVTDYFPEPVTVSWNSGALTSGVHTFP IgG1 HC AVLESSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTC Constant PPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVD Region GVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIE KTISKAKGQPREPQVYVYPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQP ENNYKTTPPVLDSDGSFALVSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQK SLSLSPGK 346 WLGCEVTDYFPEPVTVSWNSGALTSGVHTFPAVLESSGLYSLSSVVTVPSSSLGT QTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDT LMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVV SVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYVYPPSREE MTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFALV 347 90002 KASQDIHRYLS VL CDR1 348 90002 RANRLVS VL CDR2 349 90002 LQYDEFPYT VL CDR3 350 90002 DYYLH VH CDR1 351 90002 WIDPDQGDTEYAQKFQD VH CDR2 352 90002 AAYGSSSYPMDY VH CDR3 353 Rituximab RASSSVSYIH CD20 VL CDR1 354 Rituximab ATSNLAS CD20 VL CDR2 355 Rituximab QQWTSNPPT CD20 VL CDR3 356 Rituximab SYNMH CD20 VH CDR1 357 Rituximab AIYPGNGDTSYNQKFKG CD20 VH CDR2 358 Rituximab STYYGGDWYFNV CD20 VH CDR3 359 TPP-1361 QASQDIHRYLS CD47 VL CDR1 360 TPP-1361 RESRFVD CD47 VL CDR2 361 TPP-1361 LQYDEFPYT CD47 VL CDR3 362 TPP-1361 DYYLH CD47 VH CDR1 363 TPP-1361 WIDPDQGDTYYAQKFQG CD47 VH CDR2 364 TPP-1361 AYGESSYPMDY CD47 VH CDR3 365 TPP-1360 RASQDIHRYLS CD47 VL CDR1 366 TPP-1360 RESRFVD CD47 VL CDR2 367 TPP-1360 LQYDEFPYT CD47 VL CDR3 368 TPP-1360 DYYLH CD47 VH CDR1 369 TPP-1360 WIDPDQGDTYYAQKFQG CD47 VH CDR2 370 TPP-1360 AYGESSYPMDY CD47 VH CDR3 371 TPP-1367 RASQDIHRYLS CD47 VL CDR1 372 TPP-1367 RANRLVS CD47 VL CDR2 373 TPP-1367 LQYDEFPYT CD47 VL CDR3 374 TPP-1367 DYYLH CD47 VH CDR1 375 TPP-1367 WIDPDQGDTYYAQKFQG CD47 VH CDR2 376 TPP-1367 AYGESSYPMDY CD47 VH CDR3 377 TPP-1362 RASQGISSWLA CD47 VL CDR1 378 TPP-1362 AASVLES CD47 VL CDR2 379 TPP-1362 QQANSFPYT CD47 VL CDR3 380 TPP-1362 NFVMS CD47 VH CDR1 381 TPP-1362 TISGSGGSTYYADSVKG CD47 VH CDR2 382 TPP-1362 HYILRYFD CD47 VH CDR3 383 TPP-1362 DIQMTQSPSSVSASVGDRVTITCRASQGISSWLAWYQQKPGKAPKLLIYAASVL CD47 VL ESGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQANSFPYTFGQGTKLEIK 384 TPP1362 EVCILLESGGGLVQPGGSLRLSCAASGFTFPNFVMSWVRQAPGKGLEWVSTISG CD47 VH SGGSTYYADSVKGRFTISRDNSKNMLYLQMNSLRAEDTAVYYCAKHYILRYFD WLAGTLVTVSS 385 TPP-1362 DIQMTQSPSSVSASVGDRVTITCRASQGISSWLAWYQQKPGKAPKLLIYAASVLE CD47 WHOLE SGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQANSFPYTFGQGTKLEIKRTV AAPSVFIFPPSDEELKSGTASVVCWLNNFYPREAKVQWKVDNALQSGNSEESV LC TEQDSKDSTYSLSSTLELSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 386 TPP-1362 EVCILLESGGGLVQPGGSLRLSCAASGFTFPNFVMSWVRQAPGKGLEWVSTISG CD47 WHOLE SGGSTYYADSVKGRFTISRDNSKNMLYLQMNSLRAEDTAVYYCAKHYILRYFD HC WLAGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNS GALTSGVHTFPAVLKSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKV EPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHED PEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVS NKALPAPIEKTISKAKGQPREPQVYVLPPSREEMTKNQVSLLCLVKGFYPSDIA VEWESNGQPENNYLTWPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMH EALHNHYTQKSLSLSPGK 387 408_437 VL NIQMTQSPSSLSASVGDRVTITCRASQDIHRYLSWFQQKPGKVPKHLIYRANRL VSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQYDEFPYTFGGGTKVEIK 388 408_437 VH QMQLVQSGAEVKKPGSSVKVSCKASGFNIKDYYLHWVRQAPGKGLEWMGWIDP DQGDTEYAQKFQGRVTITRDRSTSTAYMELRSLRAEDTAVYYCNAAYGSSSY PMDYWGQGTLVTVSS

All publications and patents referred to herein are incorporated by reference. Various modifications and variations of the described subject matter will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific embodiments, it should be understood that the invention as claimed should not be unduly limited to these embodiments. Indeed, various modifications for carrying out the invention are obvious to those skilled in the art and are intended to be within the scope of the following claims. 

1.-42. (canceled)
 43. A bispecific antibody of IgG1 1+1 heterodimer format comprising at least one Fab portion that binds CD47 and at least one Fab portion that binds CD20; wherein the Fab portion that binds CD47 exhibits low affinity Kd for CD47, from about 0.1 μM to about 5.0 μM; and, wherein the Fab portion that binds CD20 comprises VL CDRs: SEQ ID NO:353 (CDRL1), SEQ ID NO:354 (CDRL2), and SEQ ID NO:355 (CDRL3), and, VH CDRs: SEQ ID NO:356 (CDRH1), SEQ ID NO:357 (CDRH2), and SEQ ID NO:358 (CDRH3); and, wherein the bispecific antibody selectively binds CD47 in tumor cells and binds less than 5% of CD47 on (CD20−/CD47+) normal cells.
 44. A bispecific antibody according to claim 43 that selectively binds B cells.
 45. A bispecific antibody according to claim 44 wherein the Fab portion that binds CD47 comprises a light chain (LC) region comprising SEQ ID NO:340.
 46. A bispecific: antibody according to claim 45 wherein the Fab portion that binds CD47 comprises a heavy chain (HC) region comprising SEQ ID NO:342.
 47. A bispecific antibody according to claim 44 that selectively binds malignant B cells.
 48. A bispecific antibody according to claim 46 that selectively binds malignant B cells.
 49. A bispecific: antibody according to claim 48 wherein the Fab portion that binds CD20 comprises a light chain (LC) region comprising SEQ ID NO:344.
 50. A bispecific antibody according to claim 49 wherein the Fab portion that binds CD20 comprises a heavy chain (HC) region comprising SEQ ID NO:
 346. 51. A bispecific antibody according to claim 50 wherein the Fab portion that binds CD47 comprises a light chain variable region (VL) region and a heavy chain variable region (VH) region comprising VL CDRs SEQ ID NO:347, SEQ ID NO:348, and SEQ ID NO:349; and, VH CDRs SEQ ID NO:350, SEQ ID NO:351, and SEQ ID NO:352, respectively.
 52. A bispecific antibody according to claim 51 wherein the anti-CD47 VL is derived from SEQ ID NO: 325 and exhibits 1-7 amino acid substitutions relative to SEQ ID NO:325; and wherein the anti-CD47 VH is derived from SEQ ID NO: 326 and exhibits 1-11 amino acid substitutions relative to SEQ ID NO:326.
 53. A bispecific antibody according to claim 44 wherein the Fab portion that binds CD47 comprises: (i) a light chain variable region (VL) region selected from the group consisting of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:5, SEQ ID NO:7, SEQ ID NO:9, SEQ ID NO:11, SEQ ID NO:13, SEQ ID NO:15, SEQ ID NO:17, SEQ ID NO:19, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:29, SEQ ID NO:31, SEQ ID NO:33, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:53, SEQ ID NO:55, SEQ ID NO:57, SEQ ID NO:59, SEQ ID NO:61, SEQ ID NO:63, SEQ ID NO:65, SEQ ID NO:67, SEQ ID NO:69, SEQ ID NO:71, SEQ ID NO:73, SEQ ID NO:75, SEQ ID NO:77, SEQ ID NO:79, SEQ ID NO:81, SEQ ID NO:83, SEQ ID NO:85, SEQ ID NO:87, SEQ ID NO:89, SEQ ID NO:91, SEQ ID NO:93, SEQ ID NO:95, SEQ ID NO:97, SEQ ID NO:99, SEQ ID NO:101, SEQ ID NO:103, SEQ ID NO:105, SEQ ID NO:107, SEQ ID NO:109, SEQ ID NO:111, SEQ ID NO:113, SEQ ID NO:115, SEQ ID NO:117, SEQ ID NO:119, SEQ ID NO:121, SEQ ID NO:123, SEQ ID NO:125, SEQ ID NO:127, SEQ ID NO:129, SEQ ID NO:131, SEQ ID NO:133, SEQ ID NO:135, SEQ ID NO:137, SEQ ID NO:139, SEQ ID NO:141, SEQ ID NO:143, SEQ ID NO:145, SEQ ID NO:147, SEQ ID NO:149, SEQ ID NO:151, SEQ ID NO:153, SEQ ID NO:155, SEQ ID NO:157, SEQ ID NO:159, SEQ ID NO:161, SEQ ID NO:163, SEQ ID NO:165, SEQ ID NO:167, SEQ ID NO:169, SEQ ID NO:171, SEQ ID NO:173, SEQ ID NO:175, SEQ ID NO:177, SEQ ID NO:179, SEQ ID NO:181, SEQ ID NO:183, SEQ ID NO:185, SEQ ID NO:187, SEQ ID NO:189, SEQ ID NO:191, SEQ ID NO:193, SEQ ID NO:195, SEQ ID NO:197, SEQ ID NO:199, SEQ ID NO:201, SEQ ID NO:203, SEQ ID NO:205, SEQ ID NO:207, SEQ ID NO:209, SEQ ID NO:211, SEQ ID NO:213, SEQ ID NO:215, SEQ ID NO:217, SEQ ID NO:219, SEQ ID NO:221, SEQ ID NO:223, SEQ ID NO:225, SEQ ID NO:227, SEQ ID NO:229, SEQ ID NO:231, SEQ ID NO:233, SEQ ID NO:235, SEQ ID NO:237, SEQ ID NO:239, SEQ ID NO:241, SEQ ID NO:243, SEQ ID NO:245, SEQ ID NO:247, SEQ ID NO:249, SEQ ID NO:251, SEQ ID NO:253, SEQ ID NO:255, SEQ ID NO:257, SEQ ID NO:259, SEQ ID NO:261, SEQ ID NO:263, SEQ ID NO:265, SEQ ID NO:267, SEQ ID NO:269, SEQ ID NO:271, SEQ ID NO:273, SEQ ID NO:275, SEQ ID NO:277, SEQ ID NO:279, SEQ ID NO:281, SEQ ID NO:283, SEQ ID NO:285, SEQ ID NO:287, SEQ ID NO:289, SEQ ID NO:291, SEQ ID NO:293, SEQ ID NO:295, SEQ ID NO:297, SEQ ID NO:299, SEQ ID NO:301, SEQ ID NO:303, SEQ ID NO:305, SEQ ID NO:307, SEQ ID NO:309, SEQ ID NO:311, SEQ ID NO:313, SEQ ID NO:315, SEQ ID NO:317, SEQ ID NO:319, and SEQ ID NO:321; and (ii) a heavy chain variable region (VH) region, selected from the group consisting of SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:12, SEQ ID NO:14, SEQ ID NO:16, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32, SEQ ID NO:34, SEQ ID NO:36, SEQ ID NO:38, SEQ ID NO:40, SEQ ID NO:42, SEQ ID NO:44, SEQ ID NO:46, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68, SEQ ID NO:70, SEQ ID NO:72, SEQ ID NO:74, SEQ ID NO:76, SEQ ID NO:78, SEQ ID NO:80, SEQ ID NO:82, SEQ ID NO:84, SEQ ID NO:86, SEQ ID NO:88, SEQ ID NO:90, SEQ ID NO:92, SEQ ID NO:94, SEQ ID NO:96, SEQ ID NO:98, SEQ ID NO:100, SEQ ID NO:102, SEQ ID NO:104, SEQ ID NO:106, SEQ ID NO:108, SEQ ID NO:110, SEQ ID NO:112, SEQ ID NO:114, SEQ ID NO:116, SEQ ID NO:118, SEQ ID NO:120, SEQ ID NO:122, SEQ ID NO:124, SEQ ID NO:126, SEQ ID NO:128, SEQ ID NO:130, SEQ ID NO:132, SEQ ID NO:134, SEQ ID NO:136, SEQ ID NO:138, SEQ ID NO:140, SEQ ID NO:142, SEQ ID NO:144, SEQ ID NO:146, SEQ ID NO:148, SEQ ID NO:150, SEQ ID NO:152, SEQ ID NO:154, SEQ ID NO:156, SEQ ID NO:158, SEQ ID NO:160, SEQ ID NO:162, SEQ ID NO:164, SEQ ID NO:166, SEQ ID NO:168, SEQ ID NO:170, SEQ ID NO:172, SEQ ID NO:174, SEQ ID NO:176, SEQ ID NO:178, SEQ ID NO:180, SEQ ID NO:182, SEQ ID NO:184, SEQ ID NO:186, SEQ ID NO:188, SEQ ID NO:190, SEQ ID NO:192, SEQ ID NO:194, SEQ ID NO:196, SEQ ID NO:198, SEQ ID NO:200, SEQ ID NO:202, SEQ ID NO:204, SEQ ID NO:206, SEQ ID NO:208, SEQ ID NO:210, SEQ ID NO:212, SEQ ID NO:214, SEQ ID NO:216, SEQ ID NO:218, SEQ ID NO:220, SEQ ID NO:222, SEQ ID NO:224, SEQ ID NO:226, SEQ ID NO:228, SEQ ID NO:230, SEQ ID NO:232, SEQ ID NO:234, SEQ ID NO:236, SEQ ID NO:238, SEQ ID NO:240, SEQ ID NO:242, SEQ ID NO:244, SEQ ID NO:246, SEQ ID NO:248, SEQ ID NO:250, SEQ ID NO:252, SEQ ID NO:254, SEQ ID NO:255, SEQ ID NO:258, SEQ ID NO:260, SEQ ID NO:262, SEQ ID NO:264, SEQ ID NO:266, SEQ ID NO:268, SEQ ID NO:270, SEQ ID NO:272, SEQ ID NO:274, SEQ ID NO:276, SEQ ID NO:278, SEQ ID NO:280, SEQ ID NO:282, SEQ ID NO:284, SEQ ID NO:286, SEQ ID NO:288, SEQ ID NO:290, SEQ ID NO:292, SEQ ID NO:294, SEQ ID NO:296, SEQ ID NO:298, SEQ ID NO:300, SEQ ID NO:302, SEQ ID NO:304, SEQ ID NO:306, SEQ ID NO:308, SEQ ID NO:310, SEQ ID NO:312, SEQ ID NO:314, SEQ ID NO:316, SEQ ID NO:318, SEQ ID NO:320, and SEQ ID NO:322.
 54. A bispecific antibody according to claim 50 wherein the Fab portion that binds CD4 comprises: (i) a light chain variable region (VL) region selected from the group consisting of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:5, SEQ ID NO:7, SEQ ID NO:9, SEQ ID NO:11, SEQ ID NO:13, SEQ ID NO:15, SEQ ID NO:17, SEQ ID NO:19, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:29, SEQ ID NO:31, SEQ ID NO:33, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:53, SEQ ID NO:55, SEQ ID NO:57, SEQ ID NO:59, SEQ ID NO:61, SEQ ID NO:63, SEQ ID NO:65, SEQ ID NO:67, SEQ ID NO:69, SEQ ID NO:71, SEQ ID NO:73, SEQ ID NO:75, SEQ ID NO:77, SEQ ID NO:79, SEQ ID NO:81, SEQ ID NO:83, SEQ ID NO:85, SEQ ID NO:87, SEQ ID NO:89, SEQ ID NO:91, SEQ ID NO:93, SEQ ID NO:95, SEQ ID NO:97, SEQ ID NO:99, SEQ ID NO:101, SEQ ID NO:103, SEQ ID NO:105, SEQ ID NO:107, SEQ ID NO:109, SEQ ID NO:111, SEQ ID NO:113, SEQ ID NO:115, SEQ ID NO:117, SEQ ID NO:119, SEQ ID NO:121, SEQ ID NO:123, SEQ ID NO:125, SEQ ID NO:127, SEQ ID NO:129, SEQ ID NO:131, SEQ ID NO:133, SEQ ID NO:135, SEQ ID NO:137, SEQ ID NO:139, SEQ ID NO:141, SEQ ID NO:143, SEQ ID NO:145, SEQ ID NO:147, SEQ ID NO:149, SEQ ID NO:151, SEQ ID NO:153, SEQ ID NO:155, SEQ ID NO:157, SEQ ID NO:159, SEQ ID NO:161, SEQ ID NO:163, SEQ ID NO:165, SEQ ID NO:167, SEQ ID NO:169, SEQ ID NO:171, SEQ ID NO:173, SEQ ID NO:175, SEQ ID NO:177, SEQ ID NO:179, SEQ ID NO:181, SEQ ID NO:183, SEQ ID NO:185, SEQ ID NO:187, SEQ ID NO:189, SEQ ID NO:191, SEQ ID NO:193, SEQ ID NO:195, SEQ ID NO:197, SEQ ID NO:199, SEQ ID NO:201, SEQ ID NO:203, SEQ ID NO:205, SEQ ID NO:207, SEQ ID NO:209, SEQ ID NO:211, SEQ ID NO:213, SEQ ID NO:215, SEQ ID NO:217, SEQ ID NO:219, SEQ ID NO:221, SEQ ID NO:223, SEQ ID NO:225, SEQ ID NO:227, SEQ ID NO:229, SEQ ID NO:231, SEQ ID NO:233, SEQ ID NO:235, SEQ ID NO:237, SEQ ID NO:239, SEQ ID NO:241, SEQ ID NO:243, SEQ ID NO:245, SEQ ID NO:247, SEQ ID NO:249, SEQ ID NO:251, SEQ ID NO:253, SEQ ID NO:255, SEQ ID NO:257, SEQ ID NO:259, SEQ ID NO:261, SEQ ID NO:263, SEQ ID NO:265, SEQ ID NO:267, SEQ ID NO:269, SEQ ID NO:271, SEQ ID NO:273, SEQ ID NO:275, SEQ ID NO:277, SEQ ID NO:279, SEQ ID NO:281, SEQ ID NO:283, SEQ ID NO:285, SEQ ID NO:287, SEQ ID NO:289, SEQ ID NO:291, SEQ ID NO:293, SEQ ID NO:295, SEQ ID NO:297, SEQ ID NO:299, SEQ ID NO:301, SEQ ID NO:303, SEQ ID NO:305, SEQ ID NO:307, SEQ ID NO:309, SEQ ID NO:311, SEQ ID NO:313, SEQ ID NO:315, SEQ ID NO:317, SEQ ID NO:319, and SEQ ID NO:321; and (ii) a heavy chain variable region (VH) region, selected from the group consisting of SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:12, SEQ ID NO:14, SEQ ID NO:16, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32, SEQ ID NO:34, SEQ ID NO:36, SEQ ID NO:38, SEQ ID NO:40, SEQ ID NO:42, SEQ ID NO:44, SEQ ID NO:46, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68, SEQ ID NO:70, SEQ ID NO:72, SEQ ID NO:74, SEQ ID NO:76, SEQ ID NO:78, SEQ ID NO:80, SEQ ID NO:82, SEQ ID NO:84, SEQ ID NO:86, SEQ ID NO:88, SEQ ID NO:90, SEQ ID NO:92, SEQ ID NO:94, SEQ ID NO:96, SEQ ID NO:98, SEQ ID NO:100, SEQ ID NO:102, SEQ ID NO:104, SEQ ID NO:106, SEQ ID NO:108, SEQ ID NO:110, SEQ ID NO:112, SEQ ID NO:114, SEQ ID NO:116, SEQ ID NO:118, SEQ ID NO:120, SEQ ID NO:122, SEQ ID NO:124, SEQ ID NO:126, SEQ ID NO:128, SEQ ID NO:130, SEQ ID NO:132, SEQ ID NO:134, SEQ ID NO:136, SEQ ID NO:138, SEQ ID NO:140, SEQ ID NO:142, SEQ ID NO:144, SEQ ID NO:146, SEQ ID NO:148, SEQ ID NO:150, SEQ ID NO:152, SEQ ID NO:154, SEQ ID NO:156, SEQ ID NO:158, SEQ ID NO:160, SEQ ID NO:162, SEQ ID NO:164, SEQ ID NO:166, SEQ ID NO:168, SEQ ID NO:170, SEQ ID NO:172, SEQ ID NO:174, SEQ ID NO:176, SEQ ID NO:178, SEQ ID NO:180, SEQ ID NO:182, SEQ ID NO:184, SEQ ID NO:186, SEQ ID NO:188, SEQ ID NO:190, SEQ ID NO:192, SEQ ID NO:194, SEQ ID NO:196, SEQ ID NO:198, SEQ ID NO:200, SEQ ID NO:202, SEQ ID NO:204, SEQ ID NO:206, SEQ ID NO:208, SEQ ID NO:210, SEQ ID NO:212, SEQ ID NO:214, SEQ ID NO:216, SEQ ID NO:218, SEQ ID NO:220, SEQ ID NO:222, SEQ ID NO:224, SEQ ID NO:226, SEQ ID NO:228, SEQ ID NO:230, SEQ ID NO:232, SEQ ID NO:234, SEQ ID NO:236, SEQ ID NO:238, SEQ ID NO:240, SEQ ID NO:242, SEQ ID NO:244, SEQ ID NO:246, SEQ ID NO:248, SEQ ID NO:250, SEQ ID NO:252, SEQ ID NO:254, SEQ ID NO:255, SEQ ID NO:258, SEQ ID NO:260, SEQ ID NO:262, SEQ ID NO:264, SEQ ID NO:266, SEQ ID NO:268, SEQ ID NO:270, SEQ ID NO:272, SEQ ID NO:274, SEQ ID NO:276, SEQ ID NO:278, SEQ ID NO:280, SEQ ID NO:282, SEQ ID NO:284, SEQ ID NO:286, SEQ ID NO:288, SEQ ID NO:290, SEQ ID NO:292, SEQ ID NO:294, SEQ ID NO:296, SEQ ID NO:298, SEQ ID NO:300, SEQ ID NO:302, SEQ ID NO:304, SEQ ID NO:306, SEQ ID NO:308, SEQ ID NO:310, SEQ ID NO:312, SEQ ID NO:314, SEQ ID NO:316, SEQ ID NO:318, SEQ ID NO:320, and SEQ ID NO:322.
 55. A bispecific antibody according to claim 44 wherein the Fab portion that binds CD47 comprises a light chain variable region (VL) region comprising VL CDRs QASQDIHRYLS (SEQ ID NO:359), RESRFVD (SEQ ID NO:360), and LQYDEFPYT (SEQ ID NO:361); and, a heavy chain variable region (VH) region comprising VH CDRs DYYLH (SEQ ID NO:362), WIDPDQGDTYYAQKFQG (SEQ ID NO:363), AYGESSYPMDY (SEQ ID NO:364).
 56. A bispecific antibody according to claim 44 wherein the Fab portion that binds CD47 comprises a light chain variable region (VL) region comprising VL CDRs RASQDIHRYLS (SEQ ID NO:365), RESRFVD (SEQ ID NO:366), LQYDEFPYT (SEQ ID NO:367); and, a heavy chain variable region (VH) region comprising VH CDRs DYYLH (SEQ ID NO:368), WIDPDQGDTYYAQKFQG (SEQ ID NO:369), AYGESSYPMDY (SEQ ID NO:370).
 57. A bispecific antibody according to claim 44 wherein the Fab portion that hinds CD47 comprises a light chain variable region (VL) region comprising VL CDRs RASQDIHRYLS (SEQ ID NO:371), RANRLVS (SEQ ID NO:372), LQYDEFPYT (SEQ ID NO:373); and, a heavy chain variable region (VH) region comprising VH CDRs DYYLH (SEQ ID NO:374), WIDPDQGDTYYAQKFQG (SEQ ID NO:375), AYGESSYPMDY (SEQ ID NO:376).
 58. A bispecific antibody according to claim 50 wherein the Fab portion that binds CD47 comprises a light chain variable region (VL) region comprising VL CDRs QASQDIHRYLS (SEQ ID NO:359), RESRFVD (SEQ ID NO:360), and LQYDEFPYT (SEQ ID NO:361); and, a heavy chain variable region (VH) region comprising VH CDRs DYYLH (SEQ ID NO:362), WIDPDQGDTYYAQKFQG (SEQ ID NO:363), AYGESSYPMDY (SEQ ID NO:364).
 59. A bispecific antibody according to claim 50 wherein the Fab portion that hinds CD47 comprises a light chain variable region (VL) region comprising VL CDRs RASQDIHRYLS (SEQ ID NO:365), RESRFVD (SEQ ID NO:366), LQYDEFPYT (SEQ ID NO:367); and, a heavy chain variable region (VH) region comprising VH CDRs DYYLH (SEQ ID NO:368), WIDPDQGDTYYAQKFQG (SEQ ID NO:369), AYGESSYPMDY (SEQ ID NO:370).
 60. A bispecific antibody according to claim 50 wherein the Fab portion that binds CD47 comprises a light chain variable region (VL) region comprising VL CDRs RASQDIHRYLS (SEQ ID NO:371), RANRLVS (SEQ ID NO:372), LQYDEFPYT (SEQ ID NO:373); and, a heavy chain variable region (VH) region comprising VH CDRs DYYLH (SEQ ID NO:374), WIDPDQGDTYYAQKFQG (SEQ ID NO:375), AYGESSYPMDY (SEQ ID NO:376).
 61. A bispecific antibody according to claim 55 comprising a VL region comprising SEQ ID NO:317; and, a VH region comprising SEQ ID NO:318.
 62. A bispecific antibody according to claim 56 comprising a VL region comprising SEQ ID NO:319; and, a VH region comprising SEQ ID NO:320.
 63. A bispecific antibody according to claim 57 comprising a VL region comprising SEQ ID NO:321; and, a VH region comprising SEQ ID NO:322.
 64. A bispecific antibody according to claim 58 comprising a VL region comprising SEQ ID NO:317; and, a VH region comprising SEQ ID NO:318.
 65. A bispecific antibody according to claim 59 comprising a VL region comprising SEQ ID NO:319; and, a VU region comprising SEQ ID NO:320.
 66. A bispecific antibody according to claim 60 comprising a VL region comprising SEQ ID NO:321; and, a VH region comprising SEQ ID NO:322.
 67. A bispecific antibody according to claim 52 comprising at least one (1) amino acid substitution in the anti-CD47 VL (SEQ ID NO: 325) selected from the group consisting of ATOS, M11L, K24R, A51E, N52S, L54F, and S56D.
 68. A bispecific antibody according to claim 67 comprising at least two (2) amino acid substitutions in the anti-CD47 VH (SEQ ID NO: 326) selected from the group consisting of T14P, Q43K, A44G, E59Y, D66G, M76T, S84R, S88A, M93V, S102E, and T115L.
 69. A bispecific antibody according to claim 68 comprising at least three (3) amino acid substitutions in the anti-CD47 VH (SEQ ID NO: 326) selected from the group consisting of T14P, Q43K, A44G, E59Y, D66G, M76T, S84R, S88A, M93V, S102E, and T115L.
 70. A bispecific antibody according to claim 69 comprising an anti-CD47 VL region comprising SEQ ID NO:319 and an anti-CD47 VH region comprising SEQ ID NO:320.
 71. A bispecific antibody according to claim 70 comprising an anti-CD47 LC region comprising SEQ ID NO:335 and an anti-CD47 HC region comprising SEQ ID NO:336.
 72. A bispecific antibody according to claim 50 comprising an anti-CD20 VL region comprising SEQ ID NO: 323 and a VH region comprising SEQ ID NO:
 324. 73. A bispecific antibody according to claim 72 comprising an anti-CD20 LC region comprising (SEQ ID NO:331) and an anti-CD20 HC region comprising SEQ ID NO:332.
 74. A bispecific antibody according to claim 54 comprising an anti-CD20 VL region comprising SEQ ID NO: 323 and a VH region comprising SEQ ID NO:
 324. 75. A bispecific antibody according to claim 74 comprising an anti-CD20 LC region comprising SEQ ID NO:331 and an anti-CD20 HC region comprising SEQ ID NO:332.
 76. A bispecific antibody according to claim 75 comprising an anti-CD47 LC region comprising SEQ ID NO:333 and an anti-CD47 HC region comprising SEQ ID NO:334.
 77. A bispecific antibody according to claim 75 comprising an anti-CD47 LC region comprising SEQ ID NO:335 and an anti-CD47 HC region comprising SEQ ID NO:336.
 78. A bispecific antibody according to claim 75 comprising an anti-CD47 LC region comprising SEQ ID NO:337 and an anti-CD47 HC region comprising SEQ ID NO:338.
 79. A pharmaceutical composition for administration to a patient in need thereof comprising i) the bispecific antibody of claim 43; and ii) at least one pharmaceutically acceptable carrier.
 80. A method of controlling tumor cells in a patient comprising administering an effective amount of the bispecific antibody of claim
 43. 81. A method according to claim 80 of controlling a hematological malignancy or a B-cell disorder in a patient.
 82. A method according to claim 81 of controlling a B-cell malignancy in a patient. 